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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: 15-55355385-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=55355385&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "15",
"pos": 55355385,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_004855.5",
"consequences": [
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1618T>C",
"hgvs_p": "p.Tyr540His",
"transcript": "NM_004855.5",
"protein_id": "NP_004846.4",
"transcript_support_level": null,
"aa_start": 540,
"aa_end": null,
"aa_length": 554,
"cds_start": 1618,
"cds_end": null,
"cds_length": 1665,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000164305.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_004855.5"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1618T>C",
"hgvs_p": "p.Tyr540His",
"transcript": "ENST00000164305.10",
"protein_id": "ENSP00000164305.5",
"transcript_support_level": 1,
"aa_start": 540,
"aa_end": null,
"aa_length": 554,
"cds_start": 1618,
"cds_end": null,
"cds_length": 1665,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_004855.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000164305.10"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCPG1",
"gene_hgnc_id": 24227,
"hgvs_c": "c.*835A>G",
"hgvs_p": null,
"transcript": "NM_001204450.2",
"protein_id": "NP_001191379.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 807,
"cds_start": null,
"cds_end": null,
"cds_length": 2424,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000442196.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001204450.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCPG1",
"gene_hgnc_id": 24227,
"hgvs_c": "c.*835A>G",
"hgvs_p": null,
"transcript": "ENST00000442196.8",
"protein_id": "ENSP00000403400.3",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 807,
"cds_start": null,
"cds_end": null,
"cds_length": 2424,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001204450.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000442196.8"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CCPG1",
"gene_hgnc_id": 24227,
"hgvs_c": "c.*4114A>G",
"hgvs_p": null,
"transcript": "ENST00000310958.10",
"protein_id": "ENSP00000311656.6",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 757,
"cds_start": null,
"cds_end": null,
"cds_length": 2274,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000310958.10"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1621T>C",
"hgvs_p": "p.Tyr541His",
"transcript": "ENST00000539642.5",
"protein_id": "ENSP00000438963.2",
"transcript_support_level": 5,
"aa_start": 541,
"aa_end": null,
"aa_length": 555,
"cds_start": 1621,
"cds_end": null,
"cds_length": 1668,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000539642.5"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1573T>C",
"hgvs_p": "p.Tyr525His",
"transcript": "ENST00000858252.1",
"protein_id": "ENSP00000528311.1",
"transcript_support_level": null,
"aa_start": 525,
"aa_end": null,
"aa_length": 539,
"cds_start": 1573,
"cds_end": null,
"cds_length": 1620,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858252.1"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1555T>C",
"hgvs_p": "p.Tyr519His",
"transcript": "ENST00000919400.1",
"protein_id": "ENSP00000589459.1",
"transcript_support_level": null,
"aa_start": 519,
"aa_end": null,
"aa_length": 533,
"cds_start": 1555,
"cds_end": null,
"cds_length": 1602,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000919400.1"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1525T>C",
"hgvs_p": "p.Tyr509His",
"transcript": "ENST00000946972.1",
"protein_id": "ENSP00000617031.1",
"transcript_support_level": null,
"aa_start": 509,
"aa_end": null,
"aa_length": 523,
"cds_start": 1525,
"cds_end": null,
"cds_length": 1572,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000946972.1"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1513T>C",
"hgvs_p": "p.Tyr505His",
"transcript": "ENST00000858254.1",
"protein_id": "ENSP00000528313.1",
"transcript_support_level": null,
"aa_start": 505,
"aa_end": null,
"aa_length": 519,
"cds_start": 1513,
"cds_end": null,
"cds_length": 1560,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858254.1"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1477T>C",
"hgvs_p": "p.Tyr493His",
"transcript": "ENST00000858255.1",
"protein_id": "ENSP00000528314.1",
"transcript_support_level": null,
"aa_start": 493,
"aa_end": null,
"aa_length": 507,
"cds_start": 1477,
"cds_end": null,
"cds_length": 1524,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858255.1"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1468T>C",
"hgvs_p": "p.Tyr490His",
"transcript": "ENST00000858253.1",
"protein_id": "ENSP00000528312.1",
"transcript_support_level": null,
"aa_start": 490,
"aa_end": null,
"aa_length": 504,
"cds_start": 1468,
"cds_end": null,
"cds_length": 1515,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858253.1"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1192T>C",
"hgvs_p": "p.Tyr398His",
"transcript": "ENST00000858251.1",
"protein_id": "ENSP00000528310.1",
"transcript_support_level": null,
"aa_start": 398,
"aa_end": null,
"aa_length": 412,
"cds_start": 1192,
"cds_end": null,
"cds_length": 1239,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858251.1"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1075T>C",
"hgvs_p": "p.Tyr359His",
"transcript": "ENST00000858256.1",
"protein_id": "ENSP00000528315.1",
"transcript_support_level": null,
"aa_start": 359,
"aa_end": null,
"aa_length": 373,
"cds_start": 1075,
"cds_end": null,
"cds_length": 1122,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858256.1"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1066T>C",
"hgvs_p": "p.Tyr356His",
"transcript": "ENST00000858257.1",
"protein_id": "ENSP00000528316.1",
"transcript_support_level": null,
"aa_start": 356,
"aa_end": null,
"aa_length": 370,
"cds_start": 1066,
"cds_end": null,
"cds_length": 1113,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858257.1"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.934T>C",
"hgvs_p": "p.Tyr312His",
"transcript": "ENST00000919401.1",
"protein_id": "ENSP00000589460.1",
"transcript_support_level": null,
"aa_start": 312,
"aa_end": null,
"aa_length": 326,
"cds_start": 934,
"cds_end": null,
"cds_length": 981,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000919401.1"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1573T>C",
"hgvs_p": "p.Tyr525His",
"transcript": "XM_011522235.4",
"protein_id": "XP_011520537.1",
"transcript_support_level": null,
"aa_start": 525,
"aa_end": null,
"aa_length": 539,
"cds_start": 1573,
"cds_end": null,
"cds_length": 1620,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011522235.4"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1513T>C",
"hgvs_p": "p.Tyr505His",
"transcript": "XM_011522236.4",
"protein_id": "XP_011520538.1",
"transcript_support_level": null,
"aa_start": 505,
"aa_end": null,
"aa_length": 519,
"cds_start": 1513,
"cds_end": null,
"cds_length": 1560,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011522236.4"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1219T>C",
"hgvs_p": "p.Tyr407His",
"transcript": "XM_011522237.3",
"protein_id": "XP_011520539.1",
"transcript_support_level": null,
"aa_start": 407,
"aa_end": null,
"aa_length": 421,
"cds_start": 1219,
"cds_end": null,
"cds_length": 1266,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011522237.3"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1219T>C",
"hgvs_p": "p.Tyr407His",
"transcript": "XM_017022730.1",
"protein_id": "XP_016878219.1",
"transcript_support_level": null,
"aa_start": 407,
"aa_end": null,
"aa_length": 421,
"cds_start": 1219,
"cds_end": null,
"cds_length": 1266,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017022730.1"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1219T>C",
"hgvs_p": "p.Tyr407His",
"transcript": "XM_017022731.2",
"protein_id": "XP_016878220.1",
"transcript_support_level": null,
"aa_start": 407,
"aa_end": null,
"aa_length": 421,
"cds_start": 1219,
"cds_end": null,
"cds_length": 1266,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_017022731.2"
},
{
"aa_ref": "Y",
"aa_alt": "H",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PIGB",
"gene_hgnc_id": 8959,
"hgvs_c": "c.1219T>C",
"hgvs_p": "p.Tyr407His",
"transcript": "XM_047433363.1",
"protein_id": "XP_047289319.1",
"transcript_support_level": null,
"aa_start": 407,
"aa_end": null,
"aa_length": 421,
"cds_start": 1219,
"cds_end": null,
"cds_length": 1266,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
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{
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],
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},
{
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],
"clinvar_disease": "not provided",
"clinvar_classification": "Uncertain significance",
"clinvar_review_status": "criteria provided, single submitter",
"clinvar_submissions_summary": "US:1",
"phenotype_combined": "not provided",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}