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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: 11-78573777-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=78573777&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 78573777,
"ref": "T",
"alt": "A",
"effect": "intron_variant",
"transcript": "ENST00000281038.10",
"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": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
"hgvs_p": null,
"transcript": "NM_024678.6",
"protein_id": "NP_078954.4",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 477,
"cds_start": -4,
"cds_end": null,
"cds_length": 1434,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2512,
"mane_select": "ENST00000281038.10",
"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": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
"hgvs_p": null,
"transcript": "ENST00000281038.10",
"protein_id": "ENSP00000281038.5",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 477,
"cds_start": -4,
"cds_end": null,
"cds_length": 1434,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2512,
"mane_select": "NM_024678.6",
"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": 15,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
"hgvs_p": null,
"transcript": "NM_001425299.1",
"protein_id": "NP_001412228.1",
"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": 2635,
"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": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
"hgvs_p": null,
"transcript": "ENST00000695360.1",
"protein_id": "ENSP00000511835.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 509,
"cds_start": -4,
"cds_end": null,
"cds_length": 1530,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2168,
"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": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
"hgvs_p": null,
"transcript": "NM_001425300.1",
"protein_id": "NP_001412229.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 468,
"cds_start": -4,
"cds_end": null,
"cds_length": 1407,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2485,
"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": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
"hgvs_p": null,
"transcript": "NM_001425301.1",
"protein_id": "NP_001412230.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 453,
"cds_start": -4,
"cds_end": null,
"cds_length": 1362,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2440,
"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": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
"hgvs_p": null,
"transcript": "NM_001425302.1",
"protein_id": "NP_001412231.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 450,
"cds_start": -4,
"cds_end": null,
"cds_length": 1353,
"cdna_start": null,
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"cdna_length": 2431,
"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": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
"hgvs_p": null,
"transcript": "NM_001425303.1",
"protein_id": "NP_001412232.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 441,
"cds_start": -4,
"cds_end": null,
"cds_length": 1326,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2404,
"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": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
"hgvs_p": null,
"transcript": "ENST00000695344.1",
"protein_id": "ENSP00000511819.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 441,
"cds_start": -4,
"cds_end": null,
"cds_length": 1326,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2343,
"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,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
"hgvs_p": null,
"transcript": "NM_001425304.1",
"protein_id": "NP_001412233.1",
"transcript_support_level": null,
"aa_start": null,
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"aa_length": 431,
"cds_start": -4,
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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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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": 1,
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"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
"hgvs_p": null,
"transcript": "NM_001425305.1",
"protein_id": "NP_001412234.1",
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"cds_start": -4,
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"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 14,
"intron_rank": 1,
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"gene_symbol": "NARS2",
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"hgvs_c": "c.141+571A>T",
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"transcript": "ENST00000695358.1",
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},
{
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],
"exon_rank": null,
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"intron_rank": 1,
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"gene_symbol": "NARS2",
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"hgvs_c": "c.141+571A>T",
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"transcript": "ENST00000695351.1",
"protein_id": "ENSP00000511826.1",
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},
{
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"strand": false,
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],
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"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.141+571A>T",
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"transcript": "NM_001425306.1",
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],
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"gene_symbol": "NARS2",
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},
{
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"strand": false,
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],
"exon_rank": null,
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"exon_count": 12,
"intron_rank": 1,
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"gene_symbol": "NARS2",
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"hgvs_c": "c.141+571A>T",
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},
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],
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"gene_symbol": "NARS2",
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"hgvs_c": "c.141+571A>T",
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"transcript": "NM_001425309.1",
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},
{
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],
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"exon_count": 12,
"intron_rank": 1,
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"gene_symbol": "NARS2",
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"hgvs_c": "c.141+571A>T",
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"transcript": "ENST00000695357.1",
"protein_id": "ENSP00000511832.1",
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},
{
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"protein_coding": true,
"strand": false,
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],
"exon_rank": null,
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"exon_count": 15,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.-541+1052A>T",
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"transcript": "NM_001425310.1",
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},
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],
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},
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],
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"gene_symbol": "NARS2",
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},
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"consequences": [
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],
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"intron_rank": 1,
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"gene_symbol": "NARS2",
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"hgvs_c": "c.-613+1052A>T",
"hgvs_p": null,
"transcript": "NM_001425312.1",
"protein_id": "NP_001412241.1",
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"feature": null
},
{
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"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "NARS2",
"gene_hgnc_id": 26274,
"hgvs_c": "c.-803-249A>T",
"hgvs_p": null,
"transcript": "NM_001425313.1",
"protein_id": "NP_001412242.1",
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},
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}