Ensembl rest api
Query gene, sequence, and variant data via the Ensembl REST APIFrom its SKILL.md
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Ensembl REST API Guide
Overview
Ensembl is a genome browser and annotation system maintained by EMBL-EBI and the Wellcome Sanger Institute, providing reference assemblies, gene annotations, variant data, and comparative genomics for over 300 vertebrate genomes. It is the genomic reference underpinning gget, PyEnsembl, and BioMart.
The REST API exposes Ensembl data via stateless HTTP. Researchers can look up genes by symbol or stable ID, retrieve genomic/cDNA/protein sequences, query variant annotations (rsIDs, clinical significance, consequences), access cross-references (HGNC, UniProt, RefSeq, OMIM), and obtain assembly metadata. Responses in JSON or XML.
Authentication
No authentication required. All endpoints are publicly accessible. Users needing higher throughput can register for an API token.
Core Endpoints
lookup/symbol: Gene Lookup by Symbol
Retrieve gene metadata: coordinates, biotype, canonical transcript.
- URL:
GET https://rest.ensembl.org/lookup/symbol/{species}/{symbol} - Parameters:
| Parameter | Type | Required | Description |
|---|---|---|---|
| species | string | Yes | Species name (e.g., homo_sapiens) |
| symbol | string | Yes | Gene symbol (e.g., BRCA1, TP53) |
| expand | int | No | Set to 1 to include transcripts and translations |
| content-type | string | Yes | application/json or text/xml |
- Example:
curl "https://rest.ensembl.org/lookup/symbol/homo_sapiens/BRCA1?content-type=application/json"
- Response (actual):
{
"display_name": "BRCA1",
"description": "BRCA1 DNA repair associated [Source:HGNC Symbol;Acc:HGNC:1100]",
"object_type": "Gene", "species": "homo_sapiens",
"assembly_name": "GRCh38", "biotype": "protein_coding",
"seq_region_name": "17", "start": 43044292, "end": 43170245, "strand": -1,
"id": "ENSG00000012048", "canonical_transcript": "ENST00000357654.9"
}
sequence/id: Sequence Retrieval
Retrieve genomic, cDNA, CDS, or protein sequences by Ensembl stable ID.
- URL:
GET https://rest.ensembl.org/sequence/id/{id} - Parameters:
| Parameter | Type | Required | Description |
|---|---|---|---|
| id | string | Yes | Ensembl stable ID (e.g., ENSG00000012048) |
| type | string | No | genomic, cdna, cds, or protein |
| expand_5prime | int | No | Expand 5' flanking region by N bases |
| expand_3prime | int | No | Expand 3' flanking region by N bases |
| content-type | string | Yes | application/json or text/plain (FASTA) |
- Example:
curl "https://rest.ensembl.org/sequence/id/ENSG00000012048?content-type=application/json&type=genomic"
- Response (actual, seq truncated):
{
"id": "ENSG00000012048", "query": "ENSG00000012048",
"desc": "chromosome:GRCh38:17:43044292:43170245:-1",
"molecule": "DNA",
"seq": "AAAGCGTGGGAATTACAGATAAATTAAAACTGTGGAACCCCTTTCCTCGGCTGCCGCCAAGGTGTTCGG..."
}
xrefs/symbol: Cross-References
Map a gene symbol to Ensembl stable IDs and external database identifiers.
- URL:
GET https://rest.ensembl.org/xrefs/symbol/{species}/{symbol} - Key params:
species(required),symbol(required),external_db(optional filter, e.g.,UniProt) - Example:
curl "https://rest.ensembl.org/xrefs/symbol/homo_sapiens/TP53?content-type=application/json"
- Response (actual):
[{"type":"gene","id":"ENSG00000141510"},{"type":"gene","id":"LRG_321"}]
Use xrefs/id/{id} to expand an Ensembl ID to all external cross-references (UniProt, HGNC, RefSeq, OMIM).
variation: Variant Annotation
Retrieve variant data by rsID: mappings, alleles, consequence, clinical significance.
- URL:
GET https://rest.ensembl.org/variation/{species}/{id} - Key params:
species(required),id(required, e.g.,rs699) - Example:
curl "https://rest.ensembl.org/variation/homo_sapiens/rs699?content-type=application/json"
- Response (actual, synonyms truncated):
{
"name": "rs699", "var_class": "SNP",
"most_severe_consequence": "missense_variant",
"clinical_significance": ["benign"],
"evidence": ["Frequency","1000Genomes","Cited","ESP","Phenotype_or_Disease","ExAC","TOPMed","gnomAD"],
"mappings": [{"location":"1:230710048-230710048","allele_string":"A/G","strand":1,"assembly_name":"GRCh38"}]
}
info/assembly: Assembly Metadata
- URL:
GET https://rest.ensembl.org/info/assembly/{species} - Response (actual): Returns
assembly_name("GRCh38.p14"),assembly_date("2013-12"),assembly_accession("GCA_000001405.29"), fullkaryotypearray (1-22, X, Y, MT), and 347top_level_regionentries.
Rate Limits
- Without token: 15 requests per second per IP.
- With token: higher limits available upon registration.
- Response headers:
X-RateLimit-Limit,X-RateLimit-Remaining,X-RateLimit-Reseton every response. - Batch POST endpoints (
/lookup/id,/sequence/id): accept up to 1000 IDs per request. - GRCh37 mirror:
https://grch37.rest.ensembl.org
Academic Use Cases
- Gene annotation: Look up coordinates and biotypes for HGNC symbols to annotate RNA-seq results.
- Variant interpretation: Retrieve consequence types and clinical significance for GWAS rsIDs.
- ID mapping: Map between Ensembl, UniProt, RefSeq, and HGNC identifiers.
- Primer design: Fetch genomic sequences with flanking regions for PCR or CRISPR targeting.
- Comparative genomics: Query homology endpoints for orthologs across species.
Code Examples (Python)
Gene Lookup and Sequence Retrieval
import requests
BASE = "https://rest.ensembl.org"
HEADERS = {"Content-Type": "application/json"}
gene = requests.get(f"{BASE}/lookup/symbol/homo_sapiens/BRCA1", headers=HEADERS).json()
print(f"{gene['display_name']} ({gene['id']}) chr{gene['seq_region_name']}:{gene['start']}-{gene['end']}")
seq = requests.get(f"{BASE}/sequence/id/{gene['id']}?type=cds", headers=HEADERS).json()
print(f"CDS length: {len(seq['seq'])} bp")
Batch ID Lookup (POST)
import requests
ids = ["ENSG00000012048", "ENSG00000141510", "ENSG00000157764"] # BRCA1, TP53, BRAF
resp = requests.post(
"https://rest.ensembl.org/lookup/id",
headers={"Content-Type": "application/json", "Accept": "application/json"},
json={"ids": ids}
)
for ens_id, info in resp.json().items():
print(f"{info['display_name']:10s} chr{info['seq_region_name']}:{info['start']}-{info['end']}")
Variant Annotation Pipeline
import requests
for rsid in ["rs699", "rs1042522", "rs334"]:
v = requests.get(
f"https://rest.ensembl.org/variation/homo_sapiens/{rsid}",
headers={"Content-Type": "application/json"}
).json()
loc = v["mappings"][0]["location"] if v.get("mappings") else "N/A"
print(f"{v['name']:12s} {v['var_class']:5s} {v['most_severe_consequence']:25s} {loc}")
References
- REST API docs: https://rest.ensembl.org/documentation
- Ensembl browser: https://www.ensembl.org
- gget toolkit (built on Ensembl REST): https://pachterlab.github.io/gget/
- GRCh37 archive API: https://grch37.rest.ensembl.org
What ships with it
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Gives 0 of the 12 instructions most apis services skills give in ~2.1k tokens
Counted across 448 of the 471 authors here whose files we hold, read 2026-09-06
- Use HTTP status codes semanticallyin 25 of 448, across 11 files
- Return 201 with a Location header on createin 24 of 448, across 9 files
- Name resources plural, lowercase, kebab-casein 23 of 448, across 9 files
- Configure rate limiting with limit headersin 22 of 448, across 8 files
- Paginate list endpoints with cursor or offsetin 21 of 448, across 10 files
- Version APIs in the URL pathin 21 of 448, across 11 files
- Validate request input with a schemain 21 of 448, across 7 files
- Add pagination to all list endpointsin 18 of 448, across 15 files
- Match HTTP method to the operationin 12 of 448, across 6 files
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- Limit query depth and complexityin 12 of 448, across 7 files
Said here and by no other author read
- look up genes by symbol via lookup/symbol
- retrieve sequences by stable ID via sequence/id
- map symbols to IDs via xrefs/symbol
- use xrefs/id to find external cross-references
- fetch variant annotations via variation endpoint
- get assembly metadata via info/assembly
Grouped from the skills themselves: near-identical wordings counted once, and counted by distinct author, so one author publishing three of these counts once. Length counted with cl100k_base; the agent that loads this file may tokenize it differently.