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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: 10-121812677-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=121812677&ref=G&alt=C&genome=hg38&allGenes=true"
API Response
json
{
"variants": [
{
"chr": "10",
"pos": 121812677,
"ref": "G",
"alt": "C",
"effect": "intron_variant",
"transcript": "ENST00000224652.12",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1258-22388C>G",
"hgvs_p": null,
"transcript": "NM_001001976.3",
"protein_id": "NP_001001976.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 518,
"cds_start": -4,
"cds_end": null,
"cds_length": 1557,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4895,
"mane_select": "ENST00000224652.12",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1258-22388C>G",
"hgvs_p": null,
"transcript": "ENST00000224652.12",
"protein_id": "ENSP00000224652.6",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 518,
"cds_start": -4,
"cds_end": null,
"cds_length": 1557,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4895,
"mane_select": "NM_001001976.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1258-22388C>G",
"hgvs_p": null,
"transcript": "ENST00000369043.8",
"protein_id": "ENSP00000358039.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 518,
"cds_start": -4,
"cds_end": null,
"cds_length": 1557,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4895,
"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": 10,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "n.*975-22388C>G",
"hgvs_p": null,
"transcript": "ENST00000423243.7",
"protein_id": "ENSP00000397787.2",
"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": 2040,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1438-22388C>G",
"hgvs_p": null,
"transcript": "NM_001439361.1",
"protein_id": "NP_001426290.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 578,
"cds_start": -4,
"cds_end": null,
"cds_length": 1737,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5426,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1387-22388C>G",
"hgvs_p": null,
"transcript": "NM_001437419.1",
"protein_id": "NP_001424348.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 561,
"cds_start": -4,
"cds_end": null,
"cds_length": 1686,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5024,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1387-22388C>G",
"hgvs_p": null,
"transcript": "ENST00000690355.1",
"protein_id": "ENSP00000510433.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 561,
"cds_start": -4,
"cds_end": null,
"cds_length": 1686,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5059,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1372-22388C>G",
"hgvs_p": null,
"transcript": "ENST00000687089.1",
"protein_id": "ENSP00000510151.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 556,
"cds_start": -4,
"cds_end": null,
"cds_length": 1671,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5044,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1366-22388C>G",
"hgvs_p": null,
"transcript": "NM_001439362.1",
"protein_id": "NP_001426291.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 554,
"cds_start": -4,
"cds_end": null,
"cds_length": 1665,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4953,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1354-22388C>G",
"hgvs_p": null,
"transcript": "NM_001439363.1",
"protein_id": "NP_001426292.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 550,
"cds_start": -4,
"cds_end": null,
"cds_length": 1653,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4991,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1333-22388C>G",
"hgvs_p": null,
"transcript": "NM_001439364.1",
"protein_id": "NP_001426293.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 543,
"cds_start": -4,
"cds_end": null,
"cds_length": 1632,
"cdna_start": null,
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"cdna_length": 4920,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 13,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1330-22388C>G",
"hgvs_p": null,
"transcript": "ENST00000691830.1",
"protein_id": "ENSP00000509345.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 542,
"cds_start": -4,
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"cds_length": 1629,
"cdna_start": 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": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 10,
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"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1324-22388C>G",
"hgvs_p": null,
"transcript": "NM_001439365.1",
"protein_id": "NP_001426294.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": -4,
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"cdna_start": 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": 12,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1309-22388C>G",
"hgvs_p": null,
"transcript": "NM_001439366.1",
"protein_id": "NP_001426295.1",
"transcript_support_level": null,
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 10,
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"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1309-22388C>G",
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"transcript": "NM_001439367.1",
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"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 12,
"intron_rank": 10,
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"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1258-22388C>G",
"hgvs_p": null,
"transcript": "NM_007041.4",
"protein_id": "NP_008972.2",
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},
{
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],
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"gene_symbol": "ATE1",
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"hgvs_c": "c.1258-22388C>G",
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"transcript": "ENST00000685007.1",
"protein_id": "ENSP00000508990.1",
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"feature": null
},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 11,
"intron_rank": 9,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1158-22388C>G",
"hgvs_p": null,
"transcript": "ENST00000693486.1",
"protein_id": "ENSP00000510184.1",
"transcript_support_level": null,
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 12,
"intron_rank": 10,
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"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1237-22388C>G",
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"transcript": "NM_001288736.2",
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},
{
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],
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"gene_symbol": "ATE1",
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"hgvs_c": "c.1237-22388C>G",
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"transcript": "NM_001439368.1",
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{
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],
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"intron_rank": 10,
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"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1237-22388C>G",
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"transcript": "ENST00000540606.7",
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
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"exon_count": 12,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1237-22388C>G",
"hgvs_p": null,
"transcript": "ENST00000689571.1",
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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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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "ATE1",
"gene_hgnc_id": 782,
"hgvs_c": "c.1258-22388C>G",
"hgvs_p": null,
"transcript": "ENST00000685072.1",
"protein_id": "ENSP00000510276.1",
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}