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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: 12-89591004-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=89591004&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 89591004,
"ref": "T",
"alt": "G",
"effect": "missense_variant",
"transcript": "NM_001366524.1",
"consequences": [
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3643A>C",
"hgvs_p": "p.Ser1215Arg",
"transcript": "NM_001366521.1",
"protein_id": "NP_001353450.1",
"transcript_support_level": null,
"aa_start": 1215,
"aa_end": null,
"aa_length": 1220,
"cds_start": 3643,
"cds_end": null,
"cds_length": 3663,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000428670.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001366521.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3643A>C",
"hgvs_p": "p.Ser1215Arg",
"transcript": "ENST00000428670.8",
"protein_id": "ENSP00000392043.3",
"transcript_support_level": 5,
"aa_start": 1215,
"aa_end": null,
"aa_length": 1220,
"cds_start": 3643,
"cds_end": null,
"cds_length": 3663,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001366521.1",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000428670.8"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3757A>C",
"hgvs_p": "p.Ser1253Arg",
"transcript": "ENST00000960959.1",
"protein_id": "ENSP00000631018.1",
"transcript_support_level": null,
"aa_start": 1253,
"aa_end": null,
"aa_length": 1258,
"cds_start": 3757,
"cds_end": null,
"cds_length": 3777,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960959.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3757A>C",
"hgvs_p": "p.Ser1253Arg",
"transcript": "ENST00000960960.1",
"protein_id": "ENSP00000631019.1",
"transcript_support_level": null,
"aa_start": 1253,
"aa_end": null,
"aa_length": 1258,
"cds_start": 3757,
"cds_end": null,
"cds_length": 3777,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960960.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3730A>C",
"hgvs_p": "p.Ser1244Arg",
"transcript": "NM_001366524.1",
"protein_id": "NP_001353453.1",
"transcript_support_level": null,
"aa_start": 1244,
"aa_end": null,
"aa_length": 1249,
"cds_start": 3730,
"cds_end": null,
"cds_length": 3750,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001366524.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3730A>C",
"hgvs_p": "p.Ser1244Arg",
"transcript": "NM_001366525.1",
"protein_id": "NP_001353454.1",
"transcript_support_level": null,
"aa_start": 1244,
"aa_end": null,
"aa_length": 1249,
"cds_start": 3730,
"cds_end": null,
"cds_length": 3750,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001366525.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3643A>C",
"hgvs_p": "p.Ser1215Arg",
"transcript": "NM_001366520.1",
"protein_id": "NP_001353449.1",
"transcript_support_level": null,
"aa_start": 1215,
"aa_end": null,
"aa_length": 1220,
"cds_start": 3643,
"cds_end": null,
"cds_length": 3663,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001366520.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3643A>C",
"hgvs_p": "p.Ser1215Arg",
"transcript": "NM_001366522.1",
"protein_id": "NP_001353451.1",
"transcript_support_level": null,
"aa_start": 1215,
"aa_end": null,
"aa_length": 1220,
"cds_start": 3643,
"cds_end": null,
"cds_length": 3663,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001366522.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3643A>C",
"hgvs_p": "p.Ser1215Arg",
"transcript": "NM_001413046.1",
"protein_id": "NP_001399975.1",
"transcript_support_level": null,
"aa_start": 1215,
"aa_end": null,
"aa_length": 1220,
"cds_start": 3643,
"cds_end": null,
"cds_length": 3663,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001413046.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3643A>C",
"hgvs_p": "p.Ser1215Arg",
"transcript": "NM_001413047.1",
"protein_id": "NP_001399976.1",
"transcript_support_level": null,
"aa_start": 1215,
"aa_end": null,
"aa_length": 1220,
"cds_start": 3643,
"cds_end": null,
"cds_length": 3663,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001413047.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3643A>C",
"hgvs_p": "p.Ser1215Arg",
"transcript": "NM_001682.3",
"protein_id": "NP_001673.2",
"transcript_support_level": null,
"aa_start": 1215,
"aa_end": null,
"aa_length": 1220,
"cds_start": 3643,
"cds_end": null,
"cds_length": 3663,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001682.3"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3643A>C",
"hgvs_p": "p.Ser1215Arg",
"transcript": "ENST00000900650.1",
"protein_id": "ENSP00000570709.1",
"transcript_support_level": null,
"aa_start": 1215,
"aa_end": null,
"aa_length": 1220,
"cds_start": 3643,
"cds_end": null,
"cds_length": 3663,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000900650.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3643A>C",
"hgvs_p": "p.Ser1215Arg",
"transcript": "ENST00000939929.1",
"protein_id": "ENSP00000609988.1",
"transcript_support_level": null,
"aa_start": 1215,
"aa_end": null,
"aa_length": 1220,
"cds_start": 3643,
"cds_end": null,
"cds_length": 3663,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000939929.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 22,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3643A>C",
"hgvs_p": "p.Ser1215Arg",
"transcript": "ENST00000939931.1",
"protein_id": "ENSP00000609990.1",
"transcript_support_level": null,
"aa_start": 1215,
"aa_end": null,
"aa_length": 1220,
"cds_start": 3643,
"cds_end": null,
"cds_length": 3663,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000939931.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3637A>C",
"hgvs_p": "p.Ser1213Arg",
"transcript": "ENST00000939930.1",
"protein_id": "ENSP00000609989.1",
"transcript_support_level": null,
"aa_start": 1213,
"aa_end": null,
"aa_length": 1218,
"cds_start": 3637,
"cds_end": null,
"cds_length": 3657,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000939930.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3604A>C",
"hgvs_p": "p.Ser1202Arg",
"transcript": "NM_001413048.1",
"protein_id": "NP_001399977.1",
"transcript_support_level": null,
"aa_start": 1202,
"aa_end": null,
"aa_length": 1207,
"cds_start": 3604,
"cds_end": null,
"cds_length": 3624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001413048.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3535A>C",
"hgvs_p": "p.Ser1179Arg",
"transcript": "NM_001413049.1",
"protein_id": "NP_001399978.1",
"transcript_support_level": null,
"aa_start": 1179,
"aa_end": null,
"aa_length": 1184,
"cds_start": 3535,
"cds_end": null,
"cds_length": 3555,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001413049.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3535A>C",
"hgvs_p": "p.Ser1179Arg",
"transcript": "NM_001413050.1",
"protein_id": "NP_001399979.1",
"transcript_support_level": null,
"aa_start": 1179,
"aa_end": null,
"aa_length": 1184,
"cds_start": 3535,
"cds_end": null,
"cds_length": 3555,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001413050.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 21,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3514A>C",
"hgvs_p": "p.Ser1172Arg",
"transcript": "ENST00000960961.1",
"protein_id": "ENSP00000631020.1",
"transcript_support_level": null,
"aa_start": 1172,
"aa_end": null,
"aa_length": 1177,
"cds_start": 3514,
"cds_end": null,
"cds_length": 3534,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960961.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3502A>C",
"hgvs_p": "p.Ser1168Arg",
"transcript": "NM_001413051.1",
"protein_id": "NP_001399980.1",
"transcript_support_level": null,
"aa_start": 1168,
"aa_end": null,
"aa_length": 1173,
"cds_start": 3502,
"cds_end": null,
"cds_length": 3522,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001413051.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3502A>C",
"hgvs_p": "p.Ser1168Arg",
"transcript": "NM_001413052.1",
"protein_id": "NP_001399981.1",
"transcript_support_level": null,
"aa_start": 1168,
"aa_end": null,
"aa_length": 1173,
"cds_start": 3502,
"cds_end": null,
"cds_length": 3522,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001413052.1"
},
{
"aa_ref": "S",
"aa_alt": "R",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ATP2B1",
"gene_hgnc_id": 814,
"hgvs_c": "c.3502A>C",
"hgvs_p": "p.Ser1168Arg",
"transcript": "ENST00000939932.1",
"protein_id": "ENSP00000609991.1",
"transcript_support_level": null,
"aa_start": 1168,
"aa_end": null,
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"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
}