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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: 1-7664046-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=1&pos=7664046&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "1",
"pos": 7664046,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "ENST00000303635.12",
"consequences": [
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1499G>A",
"hgvs_p": "p.Gly500Asp",
"transcript": "NM_015215.4",
"protein_id": "NP_056030.1",
"transcript_support_level": null,
"aa_start": 500,
"aa_end": null,
"aa_length": 1673,
"cds_start": 1499,
"cds_end": null,
"cds_length": 5022,
"cdna_start": 1576,
"cdna_end": null,
"cdna_length": 8314,
"mane_select": "ENST00000303635.12",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1499G>A",
"hgvs_p": "p.Gly500Asp",
"transcript": "ENST00000303635.12",
"protein_id": "ENSP00000306522.6",
"transcript_support_level": 1,
"aa_start": 500,
"aa_end": null,
"aa_length": 1673,
"cds_start": 1499,
"cds_end": null,
"cds_length": 5022,
"cdna_start": 1576,
"cdna_end": null,
"cdna_length": 8314,
"mane_select": "NM_015215.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1499G>A",
"hgvs_p": "p.Gly500Asp",
"transcript": "ENST00000476864.2",
"protein_id": "ENSP00000452319.2",
"transcript_support_level": 1,
"aa_start": 500,
"aa_end": null,
"aa_length": 1560,
"cds_start": 1499,
"cds_end": null,
"cds_length": 4683,
"cdna_start": 1512,
"cdna_end": null,
"cdna_length": 6282,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1409G>A",
"hgvs_p": "p.Gly470Asp",
"transcript": "NM_001349608.2",
"protein_id": "NP_001336537.1",
"transcript_support_level": null,
"aa_start": 470,
"aa_end": null,
"aa_length": 1643,
"cds_start": 1409,
"cds_end": null,
"cds_length": 4932,
"cdna_start": 1506,
"cdna_end": null,
"cdna_length": 8244,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1499G>A",
"hgvs_p": "p.Gly500Asp",
"transcript": "NM_001349609.2",
"protein_id": "NP_001336538.1",
"transcript_support_level": null,
"aa_start": 500,
"aa_end": null,
"aa_length": 1567,
"cds_start": 1499,
"cds_end": null,
"cds_length": 4704,
"cdna_start": 1576,
"cdna_end": null,
"cdna_length": 7965,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1499G>A",
"hgvs_p": "p.Gly500Asp",
"transcript": "NM_001349610.2",
"protein_id": "NP_001336539.1",
"transcript_support_level": null,
"aa_start": 500,
"aa_end": null,
"aa_length": 1565,
"cds_start": 1499,
"cds_end": null,
"cds_length": 4698,
"cdna_start": 1576,
"cdna_end": null,
"cdna_length": 7990,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1499G>A",
"hgvs_p": "p.Gly500Asp",
"transcript": "NM_001410737.1",
"protein_id": "NP_001397666.1",
"transcript_support_level": null,
"aa_start": 500,
"aa_end": null,
"aa_length": 1560,
"cds_start": 1499,
"cds_end": null,
"cds_length": 4683,
"cdna_start": 1576,
"cdna_end": null,
"cdna_length": 7944,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1409G>A",
"hgvs_p": "p.Gly470Asp",
"transcript": "NM_001349612.2",
"protein_id": "NP_001336541.1",
"transcript_support_level": null,
"aa_start": 470,
"aa_end": null,
"aa_length": 1537,
"cds_start": 1409,
"cds_end": null,
"cds_length": 4614,
"cdna_start": 1506,
"cdna_end": null,
"cdna_length": 7926,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1409G>A",
"hgvs_p": "p.Gly470Asp",
"transcript": "ENST00000700415.1",
"protein_id": "ENSP00000514979.1",
"transcript_support_level": null,
"aa_start": 470,
"aa_end": null,
"aa_length": 1537,
"cds_start": 1409,
"cds_end": null,
"cds_length": 4614,
"cdna_start": 1463,
"cdna_end": null,
"cdna_length": 5986,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1427G>A",
"hgvs_p": "p.Gly476Asp",
"transcript": "NM_001410738.1",
"protein_id": "NP_001397667.1",
"transcript_support_level": null,
"aa_start": 476,
"aa_end": null,
"aa_length": 1536,
"cds_start": 1427,
"cds_end": null,
"cds_length": 4611,
"cdna_start": 1504,
"cdna_end": null,
"cdna_length": 7872,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1427G>A",
"hgvs_p": "p.Gly476Asp",
"transcript": "ENST00000700417.1",
"protein_id": "ENSP00000514981.1",
"transcript_support_level": null,
"aa_start": 476,
"aa_end": null,
"aa_length": 1536,
"cds_start": 1427,
"cds_end": null,
"cds_length": 4611,
"cdna_start": 1427,
"cdna_end": null,
"cdna_length": 5929,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1499G>A",
"hgvs_p": "p.Gly500Asp",
"transcript": "XM_011541083.3",
"protein_id": "XP_011539385.1",
"transcript_support_level": null,
"aa_start": 500,
"aa_end": null,
"aa_length": 1680,
"cds_start": 1499,
"cds_end": null,
"cds_length": 5043,
"cdna_start": 1576,
"cdna_end": null,
"cdna_length": 8304,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1499G>A",
"hgvs_p": "p.Gly500Asp",
"transcript": "XM_011541084.3",
"protein_id": "XP_011539386.1",
"transcript_support_level": null,
"aa_start": 500,
"aa_end": null,
"aa_length": 1680,
"cds_start": 1499,
"cds_end": null,
"cds_length": 5043,
"cdna_start": 1576,
"cdna_end": null,
"cdna_length": 8335,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1487G>A",
"hgvs_p": "p.Gly496Asp",
"transcript": "XM_047415988.1",
"protein_id": "XP_047271944.1",
"transcript_support_level": null,
"aa_start": 496,
"aa_end": null,
"aa_length": 1676,
"cds_start": 1487,
"cds_end": null,
"cds_length": 5031,
"cdna_start": 2322,
"cdna_end": null,
"cdna_length": 9050,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1499G>A",
"hgvs_p": "p.Gly500Asp",
"transcript": "XM_011541086.4",
"protein_id": "XP_011539388.1",
"transcript_support_level": null,
"aa_start": 500,
"aa_end": null,
"aa_length": 1673,
"cds_start": 1499,
"cds_end": null,
"cds_length": 5022,
"cdna_start": 1576,
"cdna_end": null,
"cdna_length": 8283,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1499G>A",
"hgvs_p": "p.Gly500Asp",
"transcript": "XM_017000774.3",
"protein_id": "XP_016856263.1",
"transcript_support_level": null,
"aa_start": 500,
"aa_end": null,
"aa_length": 1661,
"cds_start": 1499,
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"cdna_start": 1576,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1427G>A",
"hgvs_p": "p.Gly476Asp",
"transcript": "XM_011541087.3",
"protein_id": "XP_011539389.1",
"transcript_support_level": null,
"aa_start": 476,
"aa_end": null,
"aa_length": 1656,
"cds_start": 1427,
"cds_end": null,
"cds_length": 4971,
"cdna_start": 1504,
"cdna_end": null,
"cdna_length": 8232,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1499G>A",
"hgvs_p": "p.Gly500Asp",
"transcript": "XM_047415993.1",
"protein_id": "XP_047271949.1",
"transcript_support_level": null,
"aa_start": 500,
"aa_end": null,
"aa_length": 1654,
"cds_start": 1499,
"cds_end": null,
"cds_length": 4965,
"cdna_start": 1576,
"cdna_end": null,
"cdna_length": 7418,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1409G>A",
"hgvs_p": "p.Gly470Asp",
"transcript": "XM_011541088.3",
"protein_id": "XP_011539390.1",
"transcript_support_level": null,
"aa_start": 470,
"aa_end": null,
"aa_length": 1650,
"cds_start": 1409,
"cds_end": null,
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"cdna_start": 1506,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1427G>A",
"hgvs_p": "p.Gly476Asp",
"transcript": "XM_047415997.1",
"protein_id": "XP_047271953.1",
"transcript_support_level": null,
"aa_start": 476,
"aa_end": null,
"aa_length": 1649,
"cds_start": 1427,
"cds_end": null,
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"cdna_start": 1504,
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"cdna_length": 8211,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1409G>A",
"hgvs_p": "p.Gly470Asp",
"transcript": "XM_047415999.1",
"protein_id": "XP_047271955.1",
"transcript_support_level": null,
"aa_start": 470,
"aa_end": null,
"aa_length": 1643,
"cds_start": 1409,
"cds_end": null,
"cds_length": 4932,
"cdna_start": 1506,
"cdna_end": null,
"cdna_length": 8213,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
"hgvs_c": "c.1337G>A",
"hgvs_p": "p.Gly446Asp",
"transcript": "XM_047416005.1",
"protein_id": "XP_047271961.1",
"transcript_support_level": null,
"aa_start": 446,
"aa_end": null,
"aa_length": 1619,
"cds_start": 1337,
"cds_end": null,
"cds_length": 4860,
"cdna_start": 1434,
"cdna_end": null,
"cdna_length": 8141,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "G",
"aa_alt": "D",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CAMTA1",
"gene_hgnc_id": 18806,
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}
],
"message": null
}