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GeneBe API Showcase
This page demonstrates how to use the GeneBe API to query variant information. The API provides programmatic access to genomic annotations and variant data.
API presented here should be used for checking single variants. If you want to check many variants at once, please use other API endpoints that you will find in the documentation.
Documentation & Advanced Usage
• Complete API documentation:docs.genebe.net/docs/api/overview/
• Interactive endpoint tester:api.genebe.net/cloud/gb-api-doc/swagger-ui/
• Python client for pandas:pypi.org/project/genebe/
• Java CLI for VCF files:github.com/pstawinski/genebe-cli
• All tools documented at:docs.genebe.net
API Request Examples for Variant: 7-33357950-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=7&pos=33357950&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "7",
"pos": 33357950,
"ref": "A",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000242067.11",
"consequences": [
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1648A>G",
"hgvs_p": "p.Ile550Val",
"transcript": "NM_198428.3",
"protein_id": "NP_940820.1",
"transcript_support_level": null,
"aa_start": 550,
"aa_end": null,
"aa_length": 887,
"cds_start": 1648,
"cds_end": null,
"cds_length": 2664,
"cdna_start": 2137,
"cdna_end": null,
"cdna_length": 3996,
"mane_select": "ENST00000242067.11",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1648A>G",
"hgvs_p": "p.Ile550Val",
"transcript": "ENST00000242067.11",
"protein_id": "ENSP00000242067.6",
"transcript_support_level": 1,
"aa_start": 550,
"aa_end": null,
"aa_length": 887,
"cds_start": 1648,
"cds_end": null,
"cds_length": 2664,
"cdna_start": 2137,
"cdna_end": null,
"cdna_length": 3996,
"mane_select": "NM_198428.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.346A>G",
"hgvs_p": "p.Ile116Val",
"transcript": "ENST00000434373.3",
"protein_id": "ENSP00000388114.1",
"transcript_support_level": 1,
"aa_start": 116,
"aa_end": null,
"aa_length": 453,
"cds_start": 346,
"cds_end": null,
"cds_length": 1362,
"cdna_start": 347,
"cdna_end": null,
"cdna_length": 1982,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "n.*409A>G",
"hgvs_p": null,
"transcript": "ENST00000433714.5",
"protein_id": "ENSP00000412159.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3705,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "n.*409A>G",
"hgvs_p": null,
"transcript": "ENST00000433714.5",
"protein_id": "ENSP00000412159.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3705,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1771A>G",
"hgvs_p": "p.Ile591Val",
"transcript": "ENST00000671871.1",
"protein_id": "ENSP00000499908.1",
"transcript_support_level": null,
"aa_start": 591,
"aa_end": null,
"aa_length": 928,
"cds_start": 1771,
"cds_end": null,
"cds_length": 2787,
"cdna_start": 2274,
"cdna_end": null,
"cdna_length": 3822,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1648A>G",
"hgvs_p": "p.Ile550Val",
"transcript": "NM_001348041.4",
"protein_id": "NP_001334970.1",
"transcript_support_level": null,
"aa_start": 550,
"aa_end": null,
"aa_length": 908,
"cds_start": 1648,
"cds_end": null,
"cds_length": 2727,
"cdna_start": 2137,
"cdna_end": null,
"cdna_length": 3712,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1648A>G",
"hgvs_p": "p.Ile550Val",
"transcript": "ENST00000673056.1",
"protein_id": "ENSP00000499989.1",
"transcript_support_level": null,
"aa_start": 550,
"aa_end": null,
"aa_length": 908,
"cds_start": 1648,
"cds_end": null,
"cds_length": 2727,
"cdna_start": 1881,
"cdna_end": null,
"cdna_length": 3456,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1648A>G",
"hgvs_p": "p.Ile550Val",
"transcript": "NM_001348036.1",
"protein_id": "NP_001334965.1",
"transcript_support_level": null,
"aa_start": 550,
"aa_end": null,
"aa_length": 887,
"cds_start": 1648,
"cds_end": null,
"cds_length": 2664,
"cdna_start": 1927,
"cdna_end": null,
"cdna_length": 3785,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1648A>G",
"hgvs_p": "p.Ile550Val",
"transcript": "NM_001348043.3",
"protein_id": "NP_001334972.1",
"transcript_support_level": null,
"aa_start": 550,
"aa_end": null,
"aa_length": 886,
"cds_start": 1648,
"cds_end": null,
"cds_length": 2661,
"cdna_start": 2137,
"cdna_end": null,
"cdna_length": 3993,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1633A>G",
"hgvs_p": "p.Ile545Val",
"transcript": "NM_001033605.2",
"protein_id": "NP_001028777.1",
"transcript_support_level": null,
"aa_start": 545,
"aa_end": null,
"aa_length": 882,
"cds_start": 1633,
"cds_end": null,
"cds_length": 2649,
"cdna_start": 2122,
"cdna_end": null,
"cdna_length": 3981,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1633A>G",
"hgvs_p": "p.Ile545Val",
"transcript": "ENST00000355070.6",
"protein_id": "ENSP00000347182.2",
"transcript_support_level": 5,
"aa_start": 545,
"aa_end": null,
"aa_length": 882,
"cds_start": 1633,
"cds_end": null,
"cds_length": 2649,
"cdna_start": 2146,
"cdna_end": null,
"cdna_length": 4004,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1648A>G",
"hgvs_p": "p.Ile550Val",
"transcript": "NM_001362679.1",
"protein_id": "NP_001349608.1",
"transcript_support_level": null,
"aa_start": 550,
"aa_end": null,
"aa_length": 871,
"cds_start": 1648,
"cds_end": null,
"cds_length": 2616,
"cdna_start": 2161,
"cdna_end": null,
"cdna_length": 3625,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1648A>G",
"hgvs_p": "p.Ile550Val",
"transcript": "ENST00000671952.1",
"protein_id": "ENSP00000500239.1",
"transcript_support_level": null,
"aa_start": 550,
"aa_end": null,
"aa_length": 871,
"cds_start": 1648,
"cds_end": null,
"cds_length": 2616,
"cdna_start": 1879,
"cdna_end": null,
"cdna_length": 3237,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1543A>G",
"hgvs_p": "p.Ile515Val",
"transcript": "NM_001033604.2",
"protein_id": "NP_001028776.1",
"transcript_support_level": null,
"aa_start": 515,
"aa_end": null,
"aa_length": 852,
"cds_start": 1543,
"cds_end": null,
"cds_length": 2559,
"cdna_start": 2032,
"cdna_end": null,
"cdna_length": 3891,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1543A>G",
"hgvs_p": "p.Ile515Val",
"transcript": "ENST00000396127.6",
"protein_id": "ENSP00000379433.2",
"transcript_support_level": 5,
"aa_start": 515,
"aa_end": null,
"aa_length": 852,
"cds_start": 1543,
"cds_end": null,
"cds_length": 2559,
"cdna_start": 2056,
"cdna_end": null,
"cdna_length": 3914,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1543A>G",
"hgvs_p": "p.Ile515Val",
"transcript": "ENST00000672717.1",
"protein_id": "ENSP00000499835.1",
"transcript_support_level": null,
"aa_start": 515,
"aa_end": null,
"aa_length": 852,
"cds_start": 1543,
"cds_end": null,
"cds_length": 2559,
"cdna_start": 1719,
"cdna_end": null,
"cdna_length": 3123,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1528A>G",
"hgvs_p": "p.Ile510Val",
"transcript": "NM_014451.4",
"protein_id": "NP_055266.2",
"transcript_support_level": null,
"aa_start": 510,
"aa_end": null,
"aa_length": 847,
"cds_start": 1528,
"cds_end": null,
"cds_length": 2544,
"cdna_start": 2017,
"cdna_end": null,
"cdna_length": 3876,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1528A>G",
"hgvs_p": "p.Ile510Val",
"transcript": "ENST00000350941.7",
"protein_id": "ENSP00000313122.6",
"transcript_support_level": 5,
"aa_start": 510,
"aa_end": null,
"aa_length": 847,
"cds_start": 1528,
"cds_end": null,
"cds_length": 2544,
"cdna_start": 2041,
"cdna_end": null,
"cdna_length": 3899,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1528A>G",
"hgvs_p": "p.Ile510Val",
"transcript": "NM_001348040.3",
"protein_id": "NP_001334969.1",
"transcript_support_level": null,
"aa_start": 510,
"aa_end": null,
"aa_length": 846,
"cds_start": 1528,
"cds_end": null,
"cds_length": 2541,
"cdna_start": 2017,
"cdna_end": null,
"cdna_length": 3873,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1513A>G",
"hgvs_p": "p.Ile505Val",
"transcript": "NM_001348042.3",
"protein_id": "NP_001334971.1",
"transcript_support_level": null,
"aa_start": 505,
"aa_end": null,
"aa_length": 842,
"cds_start": 1513,
"cds_end": null,
"cds_length": 2529,
"cdna_start": 2014,
"cdna_end": null,
"cdna_length": 3873,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
"hgvs_c": "c.1513A>G",
"hgvs_p": "p.Ile505Val",
"transcript": "ENST00000671890.1",
"protein_id": "ENSP00000500146.1",
"transcript_support_level": null,
"aa_start": 505,
"aa_end": null,
"aa_length": 842,
"cds_start": 1513,
"cds_end": null,
"cds_length": 2529,
"cdna_start": 2048,
"cdna_end": null,
"cdna_length": 3243,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "I",
"aa_alt": "V",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "BBS9",
"gene_hgnc_id": 30000,
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}
],
"message": null
}