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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: 3-100752829-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=100752829&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 100752829,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001375547.2",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 66,
"exon_rank_end": null,
"exon_count": 68,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.5080A>G",
"hgvs_p": "p.Asn1694Asp",
"transcript": "NM_001375547.2",
"protein_id": "NP_001362476.1",
"transcript_support_level": null,
"aa_start": 1694,
"aa_end": null,
"aa_length": 1786,
"cds_start": 5080,
"cds_end": null,
"cds_length": 5361,
"cdna_start": 5117,
"cdna_end": null,
"cdna_length": 6737,
"mane_select": "ENST00000471714.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375547.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 66,
"exon_rank_end": null,
"exon_count": 68,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.5080A>G",
"hgvs_p": "p.Asn1694Asp",
"transcript": "ENST00000471714.6",
"protein_id": "ENSP00000420524.2",
"transcript_support_level": 5,
"aa_start": 1694,
"aa_end": null,
"aa_length": 1786,
"cds_start": 5080,
"cds_end": null,
"cds_length": 5361,
"cdna_start": 5117,
"cdna_end": null,
"cdna_length": 6737,
"mane_select": "NM_001375547.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000471714.6"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 33,
"exon_rank_end": null,
"exon_count": 35,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.2926A>G",
"hgvs_p": "p.Asn976Asp",
"transcript": "ENST00000284322.10",
"protein_id": "ENSP00000284322.6",
"transcript_support_level": 1,
"aa_start": 976,
"aa_end": null,
"aa_length": 1068,
"cds_start": 2926,
"cds_end": null,
"cds_length": 3207,
"cdna_start": 3057,
"cdna_end": null,
"cdna_length": 4498,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000284322.10"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "n.1543A>G",
"hgvs_p": null,
"transcript": "ENST00000470336.5",
"protein_id": null,
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2984,
"mane_select": null,
"mane_plus": null,
"biotype": "retained_intron",
"feature": "ENST00000470336.5"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 66,
"exon_rank_end": null,
"exon_count": 68,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.5101A>G",
"hgvs_p": "p.Asn1701Asp",
"transcript": "ENST00000710654.1",
"protein_id": "ENSP00000518403.1",
"transcript_support_level": null,
"aa_start": 1701,
"aa_end": null,
"aa_length": 1793,
"cds_start": 5101,
"cds_end": null,
"cds_length": 5382,
"cdna_start": 5117,
"cdna_end": null,
"cdna_length": 6737,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000710654.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 65,
"exon_rank_end": null,
"exon_count": 67,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.5038A>G",
"hgvs_p": "p.Asn1680Asp",
"transcript": "NM_001375550.1",
"protein_id": "NP_001362479.1",
"transcript_support_level": null,
"aa_start": 1680,
"aa_end": null,
"aa_length": 1772,
"cds_start": 5038,
"cds_end": null,
"cds_length": 5319,
"cdna_start": 5075,
"cdna_end": null,
"cdna_length": 6516,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375550.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 65,
"exon_rank_end": null,
"exon_count": 67,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.5032A>G",
"hgvs_p": "p.Asn1678Asp",
"transcript": "NM_001375549.2",
"protein_id": "NP_001362478.1",
"transcript_support_level": null,
"aa_start": 1678,
"aa_end": null,
"aa_length": 1770,
"cds_start": 5032,
"cds_end": null,
"cds_length": 5313,
"cdna_start": 5069,
"cdna_end": null,
"cdna_length": 6689,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001375549.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 63,
"exon_rank_end": null,
"exon_count": 65,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.4867A>G",
"hgvs_p": "p.Asn1623Asp",
"transcript": "NM_001349329.2",
"protein_id": "NP_001336258.2",
"transcript_support_level": null,
"aa_start": 1623,
"aa_end": null,
"aa_length": 1715,
"cds_start": 4867,
"cds_end": null,
"cds_length": 5148,
"cdna_start": 4904,
"cdna_end": null,
"cdna_length": 6345,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349329.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 61,
"exon_rank_end": null,
"exon_count": 63,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.4753A>G",
"hgvs_p": "p.Asn1585Asp",
"transcript": "ENST00000882230.1",
"protein_id": "ENSP00000552289.1",
"transcript_support_level": null,
"aa_start": 1585,
"aa_end": null,
"aa_length": 1677,
"cds_start": 4753,
"cds_end": null,
"cds_length": 5034,
"cdna_start": 4827,
"cdna_end": null,
"cdna_length": 6268,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000882230.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 60,
"exon_rank_end": null,
"exon_count": 62,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.4675A>G",
"hgvs_p": "p.Asn1559Asp",
"transcript": "ENST00000882203.1",
"protein_id": "ENSP00000552262.1",
"transcript_support_level": null,
"aa_start": 1559,
"aa_end": null,
"aa_length": 1651,
"cds_start": 4675,
"cds_end": null,
"cds_length": 4956,
"cdna_start": 4763,
"cdna_end": null,
"cdna_length": 6383,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000882203.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 60,
"exon_rank_end": null,
"exon_count": 62,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.4657A>G",
"hgvs_p": "p.Asn1553Asp",
"transcript": "NM_001349330.2",
"protein_id": "NP_001336259.2",
"transcript_support_level": null,
"aa_start": 1553,
"aa_end": null,
"aa_length": 1645,
"cds_start": 4657,
"cds_end": null,
"cds_length": 4938,
"cdna_start": 4694,
"cdna_end": null,
"cdna_length": 6135,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349330.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 56,
"exon_rank_end": null,
"exon_count": 58,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.4414A>G",
"hgvs_p": "p.Asn1472Asp",
"transcript": "ENST00000882239.1",
"protein_id": "ENSP00000552298.1",
"transcript_support_level": null,
"aa_start": 1472,
"aa_end": null,
"aa_length": 1564,
"cds_start": 4414,
"cds_end": null,
"cds_length": 4695,
"cdna_start": 4496,
"cdna_end": null,
"cdna_length": 4821,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000882239.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 55,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.4333A>G",
"hgvs_p": "p.Asn1445Asp",
"transcript": "NM_001377332.1",
"protein_id": "NP_001364261.1",
"transcript_support_level": null,
"aa_start": 1445,
"aa_end": null,
"aa_length": 1537,
"cds_start": 4333,
"cds_end": null,
"cds_length": 4614,
"cdna_start": 4370,
"cdna_end": null,
"cdna_length": 5990,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001377332.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 47,
"exon_rank_end": null,
"exon_count": 49,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.3862A>G",
"hgvs_p": "p.Asn1288Asp",
"transcript": "ENST00000882206.1",
"protein_id": "ENSP00000552265.1",
"transcript_support_level": null,
"aa_start": 1288,
"aa_end": null,
"aa_length": 1380,
"cds_start": 3862,
"cds_end": null,
"cds_length": 4143,
"cdna_start": 3976,
"cdna_end": null,
"cdna_length": 5417,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000882206.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 46,
"exon_rank_end": null,
"exon_count": 48,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.3754A>G",
"hgvs_p": "p.Asn1252Asp",
"transcript": "NM_001365642.2",
"protein_id": "NP_001352571.2",
"transcript_support_level": null,
"aa_start": 1252,
"aa_end": null,
"aa_length": 1344,
"cds_start": 3754,
"cds_end": null,
"cds_length": 4035,
"cdna_start": 3791,
"cdna_end": null,
"cdna_length": 5232,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001365642.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 43,
"exon_rank_end": null,
"exon_count": 45,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.3541A>G",
"hgvs_p": "p.Asn1181Asp",
"transcript": "ENST00000882237.1",
"protein_id": "ENSP00000552296.1",
"transcript_support_level": null,
"aa_start": 1181,
"aa_end": null,
"aa_length": 1273,
"cds_start": 3541,
"cds_end": null,
"cds_length": 3822,
"cdna_start": 3572,
"cdna_end": null,
"cdna_length": 5013,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000882237.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 41,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.3460A>G",
"hgvs_p": "p.Asn1154Asp",
"transcript": "ENST00000882199.1",
"protein_id": "ENSP00000552258.1",
"transcript_support_level": null,
"aa_start": 1154,
"aa_end": null,
"aa_length": 1246,
"cds_start": 3460,
"cds_end": null,
"cds_length": 3741,
"cdna_start": 3558,
"cdna_end": null,
"cdna_length": 5178,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000882199.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 41,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.3427A>G",
"hgvs_p": "p.Asn1143Asp",
"transcript": "ENST00000950966.1",
"protein_id": "ENSP00000621025.1",
"transcript_support_level": null,
"aa_start": 1143,
"aa_end": null,
"aa_length": 1235,
"cds_start": 3427,
"cds_end": null,
"cds_length": 3708,
"cdna_start": 3507,
"cdna_end": null,
"cdna_length": 4946,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950966.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 40,
"exon_rank_end": null,
"exon_count": 42,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.3418A>G",
"hgvs_p": "p.Asn1140Asp",
"transcript": "ENST00000950971.1",
"protein_id": "ENSP00000621030.1",
"transcript_support_level": null,
"aa_start": 1140,
"aa_end": null,
"aa_length": 1232,
"cds_start": 3418,
"cds_end": null,
"cds_length": 3699,
"cdna_start": 3490,
"cdna_end": null,
"cdna_length": 4929,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000950971.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 41,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.3406A>G",
"hgvs_p": "p.Asn1136Asp",
"transcript": "ENST00000882219.1",
"protein_id": "ENSP00000552278.1",
"transcript_support_level": null,
"aa_start": 1136,
"aa_end": null,
"aa_length": 1228,
"cds_start": 3406,
"cds_end": null,
"cds_length": 3687,
"cdna_start": 3494,
"cdna_end": null,
"cdna_length": 4933,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000882219.1"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 41,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.3388A>G",
"hgvs_p": "p.Asn1130Asp",
"transcript": "NM_001349331.2",
"protein_id": "NP_001336260.2",
"transcript_support_level": null,
"aa_start": 1130,
"aa_end": null,
"aa_length": 1222,
"cds_start": 3388,
"cds_end": null,
"cds_length": 3669,
"cdna_start": 3425,
"cdna_end": null,
"cdna_length": 4866,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349331.2"
},
{
"aa_ref": "N",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 41,
"exon_rank_end": null,
"exon_count": 43,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ABI3BP",
"gene_hgnc_id": 17265,
"hgvs_c": "c.3388A>G",
"hgvs_p": "p.Asn1130Asp",
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}
],
"message": null
}