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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: 11-8436118-A-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=8436118&ref=A&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 8436118,
"ref": "A",
"alt": "C",
"effect": "missense_variant",
"transcript": "ENST00000687296.1",
"consequences": [
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "NM_001352389.2",
"protein_id": "NP_001339318.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1580,
"cdna_end": null,
"cdna_length": 2796,
"mane_select": "ENST00000687296.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "ENST00000687296.1",
"protein_id": "ENSP00000509322.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1580,
"cdna_end": null,
"cdna_length": 2796,
"mane_select": "NM_001352389.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "ENST00000315204.5",
"protein_id": "ENSP00000320754.1",
"transcript_support_level": 1,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1492,
"cdna_end": null,
"cdna_length": 2707,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "ENST00000447869.5",
"protein_id": "ENSP00000416750.1",
"transcript_support_level": 1,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1888,
"cdna_end": null,
"cdna_length": 3103,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.234T>G",
"hgvs_p": "p.Phe78Leu",
"transcript": "ENST00000444064.6",
"protein_id": "ENSP00000415688.2",
"transcript_support_level": 1,
"aa_start": 78,
"aa_end": null,
"aa_length": 203,
"cds_start": 234,
"cds_end": null,
"cds_length": 612,
"cdna_start": 234,
"cdna_end": null,
"cdna_length": 1243,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "n.360T>G",
"hgvs_p": null,
"transcript": "ENST00000526517.1",
"protein_id": null,
"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": 921,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "NM_001289061.2",
"protein_id": "NP_001275990.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1363,
"cdna_end": null,
"cdna_length": 2579,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "NM_001352387.2",
"protein_id": "NP_001339316.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1310,
"cdna_end": null,
"cdna_length": 2526,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "NM_001352388.2",
"protein_id": "NP_001339317.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1515,
"cdna_end": null,
"cdna_length": 2731,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "NM_001352390.2",
"protein_id": "NP_001339319.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1391,
"cdna_end": null,
"cdna_length": 2607,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "NM_001352391.2",
"protein_id": "NP_001339320.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1408,
"cdna_end": null,
"cdna_length": 2624,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "NM_001352392.2",
"protein_id": "NP_001339321.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1375,
"cdna_end": null,
"cdna_length": 2591,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "NM_001352393.2",
"protein_id": "NP_001339322.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1276,
"cdna_end": null,
"cdna_length": 2492,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "NM_030906.4",
"protein_id": "NP_112168.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
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"cdna_start": 1512,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "ENST00000396672.5",
"protein_id": "ENSP00000379905.1",
"transcript_support_level": 2,
"aa_start": 323,
"aa_end": null,
"aa_length": 514,
"cds_start": 969,
"cds_end": null,
"cds_length": 1545,
"cdna_start": 1343,
"cdna_end": null,
"cdna_length": 2558,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.846T>G",
"hgvs_p": "p.Phe282Leu",
"transcript": "NM_001289058.2",
"protein_id": "NP_001275987.1",
"transcript_support_level": null,
"aa_start": 282,
"aa_end": null,
"aa_length": 473,
"cds_start": 846,
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"cdna_start": 1069,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.846T>G",
"hgvs_p": "p.Phe282Leu",
"transcript": "NM_001352394.2",
"protein_id": "NP_001339323.1",
"transcript_support_level": null,
"aa_start": 282,
"aa_end": null,
"aa_length": 473,
"cds_start": 846,
"cds_end": null,
"cds_length": 1422,
"cdna_start": 1231,
"cdna_end": null,
"cdna_length": 2447,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.846T>G",
"hgvs_p": "p.Phe282Leu",
"transcript": "NM_001352395.2",
"protein_id": "NP_001339324.1",
"transcript_support_level": null,
"aa_start": 282,
"aa_end": null,
"aa_length": 473,
"cds_start": 846,
"cds_end": null,
"cds_length": 1422,
"cdna_start": 1107,
"cdna_end": null,
"cdna_length": 2323,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.846T>G",
"hgvs_p": "p.Phe282Leu",
"transcript": "ENST00000534493.5",
"protein_id": "ENSP00000436418.1",
"transcript_support_level": 2,
"aa_start": 282,
"aa_end": null,
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"cds_start": 846,
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"cdna_start": 996,
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"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.969T>G",
"hgvs_p": "p.Phe323Leu",
"transcript": "NM_001352399.2",
"protein_id": "NP_001339328.1",
"transcript_support_level": null,
"aa_start": 323,
"aa_end": null,
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"cds_start": 969,
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"cdna_start": 1276,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.846T>G",
"hgvs_p": "p.Phe282Leu",
"transcript": "NM_001352396.2",
"protein_id": "NP_001339325.1",
"transcript_support_level": null,
"aa_start": 282,
"aa_end": null,
"aa_length": 378,
"cds_start": 846,
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"cds_length": 1137,
"cdna_start": 1026,
"cdna_end": null,
"cdna_length": 3033,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.846T>G",
"hgvs_p": "p.Phe282Leu",
"transcript": "NM_001352397.2",
"protein_id": "NP_001339326.1",
"transcript_support_level": null,
"aa_start": 282,
"aa_end": null,
"aa_length": 378,
"cds_start": 846,
"cds_end": null,
"cds_length": 1137,
"cdna_start": 1113,
"cdna_end": null,
"cdna_length": 3120,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "L",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "STK33",
"gene_hgnc_id": 14568,
"hgvs_c": "c.846T>G",
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