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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: 2-172487779-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=172487779&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 172487779,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000684293.1",
"consequences": [
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.2413G>C",
"hgvs_p": "p.Asp805His",
"transcript": "NM_001394928.1",
"protein_id": "NP_001381857.1",
"transcript_support_level": null,
"aa_start": 805,
"aa_end": null,
"aa_length": 1130,
"cds_start": 2413,
"cds_end": null,
"cds_length": 3393,
"cdna_start": 2616,
"cdna_end": null,
"cdna_length": 5803,
"mane_select": null,
"mane_plus": "ENST00000442250.6",
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.2413G>C",
"hgvs_p": "p.Asp805His",
"transcript": "ENST00000442250.6",
"protein_id": "ENSP00000406694.1",
"transcript_support_level": 5,
"aa_start": 805,
"aa_end": null,
"aa_length": 1130,
"cds_start": 2413,
"cds_end": null,
"cds_length": 3393,
"cdna_start": 2616,
"cdna_end": null,
"cdna_length": 5803,
"mane_select": null,
"mane_plus": "NM_001394928.1",
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.2296G>C",
"hgvs_p": "p.Asp766His",
"transcript": "NM_000210.4",
"protein_id": "NP_000201.2",
"transcript_support_level": null,
"aa_start": 766,
"aa_end": null,
"aa_length": 1073,
"cds_start": 2296,
"cds_end": null,
"cds_length": 3222,
"cdna_start": 2499,
"cdna_end": null,
"cdna_length": 5816,
"mane_select": "ENST00000684293.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.2296G>C",
"hgvs_p": "p.Asp766His",
"transcript": "ENST00000684293.1",
"protein_id": "ENSP00000508249.1",
"transcript_support_level": null,
"aa_start": 766,
"aa_end": null,
"aa_length": 1073,
"cds_start": 2296,
"cds_end": null,
"cds_length": 3222,
"cdna_start": 2499,
"cdna_end": null,
"cdna_length": 5816,
"mane_select": "NM_000210.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.2296G>C",
"hgvs_p": "p.Asp766His",
"transcript": "ENST00000264107.12",
"protein_id": "ENSP00000264107.8",
"transcript_support_level": 1,
"aa_start": 766,
"aa_end": null,
"aa_length": 1058,
"cds_start": 2296,
"cds_end": null,
"cds_length": 3177,
"cdna_start": 2417,
"cdna_end": null,
"cdna_length": 5488,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.2296G>C",
"hgvs_p": "p.Asp766His",
"transcript": "NM_001079818.3",
"protein_id": "NP_001073286.1",
"transcript_support_level": null,
"aa_start": 766,
"aa_end": null,
"aa_length": 1091,
"cds_start": 2296,
"cds_end": null,
"cds_length": 3276,
"cdna_start": 2499,
"cdna_end": null,
"cdna_length": 5686,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.2296G>C",
"hgvs_p": "p.Asp766His",
"transcript": "ENST00000409080.6",
"protein_id": "ENSP00000386896.1",
"transcript_support_level": 2,
"aa_start": 766,
"aa_end": null,
"aa_length": 1091,
"cds_start": 2296,
"cds_end": null,
"cds_length": 3276,
"cdna_start": 2499,
"cdna_end": null,
"cdna_length": 5686,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.2281G>C",
"hgvs_p": "p.Asp761His",
"transcript": "ENST00000458358.5",
"protein_id": "ENSP00000394169.1",
"transcript_support_level": 5,
"aa_start": 761,
"aa_end": null,
"aa_length": 1086,
"cds_start": 2281,
"cds_end": null,
"cds_length": 3261,
"cdna_start": 2281,
"cdna_end": null,
"cdna_length": 3261,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.2296G>C",
"hgvs_p": "p.Asp766His",
"transcript": "NM_001365529.2",
"protein_id": "NP_001352458.1",
"transcript_support_level": null,
"aa_start": 766,
"aa_end": null,
"aa_length": 1076,
"cds_start": 2296,
"cds_end": null,
"cds_length": 3231,
"cdna_start": 2499,
"cdna_end": null,
"cdna_length": 5641,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.2296G>C",
"hgvs_p": "p.Asp766His",
"transcript": "NM_001365530.2",
"protein_id": "NP_001352459.1",
"transcript_support_level": null,
"aa_start": 766,
"aa_end": null,
"aa_length": 1058,
"cds_start": 2296,
"cds_end": null,
"cds_length": 3177,
"cdna_start": 2499,
"cdna_end": null,
"cdna_length": 5771,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.1954G>C",
"hgvs_p": "p.Asp652His",
"transcript": "ENST00000715295.1",
"protein_id": "ENSP00000520448.1",
"transcript_support_level": null,
"aa_start": 652,
"aa_end": null,
"aa_length": 977,
"cds_start": 1954,
"cds_end": null,
"cds_length": 2934,
"cdna_start": 2531,
"cdna_end": null,
"cdna_length": 5669,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.1939G>C",
"hgvs_p": "p.Asp647His",
"transcript": "NM_001316306.2",
"protein_id": "NP_001303235.1",
"transcript_support_level": null,
"aa_start": 647,
"aa_end": null,
"aa_length": 954,
"cds_start": 1939,
"cds_end": null,
"cds_length": 2865,
"cdna_start": 2234,
"cdna_end": null,
"cdna_length": 5551,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "D",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.1939G>C",
"hgvs_p": "p.Asp647His",
"transcript": "ENST00000409532.5",
"protein_id": "ENSP00000386614.1",
"transcript_support_level": 2,
"aa_start": 647,
"aa_end": null,
"aa_length": 954,
"cds_start": 1939,
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"cds_length": 2865,
"cdna_start": 2152,
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"cdna_length": 3544,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
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"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.1954G>C",
"hgvs_p": "p.Asp652His",
"transcript": "XM_017004005.2",
"protein_id": "XP_016859494.1",
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},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.1954G>C",
"hgvs_p": "p.Asp652His",
"transcript": "XM_017004006.2",
"protein_id": "XP_016859495.1",
"transcript_support_level": null,
"aa_start": 652,
"aa_end": null,
"aa_length": 962,
"cds_start": 1954,
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"cdna_start": 2249,
"cdna_end": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
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"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.1954G>C",
"hgvs_p": "p.Asp652His",
"transcript": "XM_047444221.1",
"protein_id": "XP_047300177.1",
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ITGA6",
"gene_hgnc_id": 6142,
"hgvs_c": "c.1954G>C",
"hgvs_p": "p.Asp652His",
"transcript": "XM_047444222.1",
"protein_id": "XP_047300178.1",
"transcript_support_level": null,
"aa_start": 652,
"aa_end": null,
"aa_length": 944,
"cds_start": 1954,
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"cdna_start": 2249,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "ITGA6-AS1",
"gene_hgnc_id": 40308,
"hgvs_c": "n.769-6758C>G",
"hgvs_p": null,
"transcript": "ENST00000442417.5",
"protein_id": null,
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
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"mane_select": null,
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},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "ITGA6-AS1",
"gene_hgnc_id": 40308,
"hgvs_c": "n.532+7596C>G",
"hgvs_p": null,
"transcript": "ENST00000715602.2",
"protein_id": null,
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 3,
"intron_rank": 2,
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"gene_symbol": "ITGA6-AS1",
"gene_hgnc_id": 40308,
"hgvs_c": "n.236-6758C>G",
"hgvs_p": null,
"transcript": "ENST00000830319.1",
"protein_id": null,
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"aa_start": null,
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"feature": null
},
{
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"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"intron_rank": 2,
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"gene_symbol": "ITGA6-AS1",
"gene_hgnc_id": 40308,
"hgvs_c": "n.267+7596C>G",
"hgvs_p": null,
"transcript": "ENST00000830320.1",
"protein_id": null,
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"aa_length": null,
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"cdna_start": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "ITGA6-AS1",
"gene_hgnc_id": 40308,
"hgvs_c": "n.247-6758C>G",
"hgvs_p": null,
"transcript": "ENST00000830321.1",
"protein_id": null,
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
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"cds_length": null,
"cdna_start": null,
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"cdna_length": 536,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 4,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "PDK1-AS1",
"gene_hgnc_id": 40441,
"hgvs_c": "n.704-6758C>G",
"hgvs_p": null,
"transcript": "NR_186177.1",
"protein_id": null,
"transcript_support_level": null,
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}