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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: 10-60901153-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=60901153&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "10",
"pos": 60901153,
"ref": "T",
"alt": "C",
"effect": "intron_variant",
"transcript": "ENST00000337910.10",
"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": 11,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.297-8158A>G",
"hgvs_p": null,
"transcript": "NM_014836.5",
"protein_id": "NP_055651.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 696,
"cds_start": -4,
"cds_end": null,
"cds_length": 2091,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4411,
"mane_select": "ENST00000337910.10",
"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": 11,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.297-8158A>G",
"hgvs_p": null,
"transcript": "ENST00000337910.10",
"protein_id": "ENSP00000338671.5",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 696,
"cds_start": -4,
"cds_end": null,
"cds_length": 2091,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4411,
"mane_select": "NM_014836.5",
"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": 5,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.297-8158A>G",
"hgvs_p": null,
"transcript": "NM_001242359.2",
"protein_id": "NP_001229288.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 696,
"cds_start": -4,
"cds_end": null,
"cds_length": 2091,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4483,
"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": 5,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.297-8158A>G",
"hgvs_p": null,
"transcript": "NM_001350902.2",
"protein_id": "NP_001337831.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 696,
"cds_start": -4,
"cds_end": null,
"cds_length": 2091,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4339,
"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": 5,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.297-8158A>G",
"hgvs_p": null,
"transcript": "NM_001350903.2",
"protein_id": "NP_001337832.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 696,
"cds_start": -4,
"cds_end": null,
"cds_length": 2091,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4394,
"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": 4,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.297-8158A>G",
"hgvs_p": null,
"transcript": "NM_001350904.2",
"protein_id": "NP_001337833.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 696,
"cds_start": -4,
"cds_end": null,
"cds_length": 2091,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4293,
"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": 11,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.297-8158A>G",
"hgvs_p": null,
"transcript": "NM_001350905.2",
"protein_id": "NP_001337834.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 696,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
"cdna_end": null,
"cdna_length": 4273,
"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": 5,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.297-8158A>G",
"hgvs_p": null,
"transcript": "ENST00000357917.4",
"protein_id": "ENSP00000350595.4",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 696,
"cds_start": -4,
"cds_end": null,
"cds_length": 2091,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4339,
"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": 5,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.-121-2423A>G",
"hgvs_p": null,
"transcript": "NM_001350906.2",
"protein_id": "NP_001337835.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 576,
"cds_start": -4,
"cds_end": null,
"cds_length": 1731,
"cdna_start": null,
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"cdna_length": 4451,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 13,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.-121-2423A>G",
"hgvs_p": null,
"transcript": "NM_001350907.2",
"protein_id": "NP_001337836.1",
"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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"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": 4,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.-121-2423A>G",
"hgvs_p": null,
"transcript": "NM_001350908.2",
"protein_id": "NP_001337837.1",
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},
{
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"consequences": [
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],
"exon_rank": null,
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"gene_symbol": "RHOBTB1",
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"transcript": "NM_001350909.2",
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},
{
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"consequences": [
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],
"exon_rank": null,
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"gene_symbol": "RHOBTB1",
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"hgvs_c": "c.-64-8158A>G",
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"transcript": "NM_001350910.2",
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},
{
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],
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"gene_symbol": "RHOBTB1",
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},
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],
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"transcript": "XM_006718085.2",
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},
{
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],
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"gene_symbol": "RHOBTB1",
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],
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"gene_symbol": "RHOBTB1",
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"hgvs_c": "c.297-8158A>G",
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},
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],
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"intron_rank": 6,
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"gene_symbol": "RHOBTB1",
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"hgvs_c": "c.297-8158A>G",
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"transcript": "XM_024448270.2",
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],
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],
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},
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"strand": false,
"consequences": [
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],
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"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "RHOBTB1",
"gene_hgnc_id": 18738,
"hgvs_c": "c.297-8158A>G",
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"transcript": "XM_047426074.1",
"protein_id": "XP_047282030.1",
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},
{
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"consequences": [
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],
"exon_rank": null,
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"gene_symbol": "RHOBTB1",
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"hgvs_c": "c.297-8158A>G",
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"transcript": "XM_047426075.1",
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}