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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: 9-79600997-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=79600997&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 79600997,
"ref": "C",
"alt": "A",
"effect": "intron_variant",
"transcript": "ENST00000376552.8",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TLE4",
"gene_hgnc_id": 11840,
"hgvs_c": "c.253-11659C>A",
"hgvs_p": null,
"transcript": "NM_007005.6",
"protein_id": "NP_008936.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 773,
"cds_start": -4,
"cds_end": null,
"cds_length": 2322,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4886,
"mane_select": "ENST00000376552.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TLE4",
"gene_hgnc_id": 11840,
"hgvs_c": "c.253-11659C>A",
"hgvs_p": null,
"transcript": "ENST00000376552.8",
"protein_id": "ENSP00000365735.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 773,
"cds_start": -4,
"cds_end": null,
"cds_length": 2322,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4886,
"mane_select": "NM_007005.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TLE4",
"gene_hgnc_id": 11840,
"hgvs_c": "c.253-11659C>A",
"hgvs_p": null,
"transcript": "ENST00000376537.8",
"protein_id": "ENSP00000365720.4",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 805,
"cds_start": -4,
"cds_end": null,
"cds_length": 2418,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2793,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TLE4",
"gene_hgnc_id": 11840,
"hgvs_c": "c.253-11659C>A",
"hgvs_p": null,
"transcript": "ENST00000376544.7",
"protein_id": "ENSP00000365727.4",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 704,
"cds_start": -4,
"cds_end": null,
"cds_length": 2115,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4871,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TLE4",
"gene_hgnc_id": 11840,
"hgvs_c": "n.253-418C>A",
"hgvs_p": null,
"transcript": "ENST00000470872.5",
"protein_id": "ENSP00000417245.1",
"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": 2832,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TLE4",
"gene_hgnc_id": 11840,
"hgvs_c": "c.253-11659C>A",
"hgvs_p": null,
"transcript": "NM_001282748.2",
"protein_id": "NP_001269677.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 805,
"cds_start": -4,
"cds_end": null,
"cds_length": 2418,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4982,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TLE4",
"gene_hgnc_id": 11840,
"hgvs_c": "c.253-11659C>A",
"hgvs_p": null,
"transcript": "NM_001351541.2",
"protein_id": "NP_001338470.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 786,
"cds_start": -4,
"cds_end": null,
"cds_length": 2361,
"cdna_start": null,
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"cdna_length": 4925,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TLE4",
"gene_hgnc_id": 11840,
"hgvs_c": "c.253-11659C>A",
"hgvs_p": null,
"transcript": "NM_001351542.2",
"protein_id": "NP_001338471.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 774,
"cds_start": -4,
"cds_end": null,
"cds_length": 2325,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4889,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TLE4",
"gene_hgnc_id": 11840,
"hgvs_c": "c.247-11659C>A",
"hgvs_p": null,
"transcript": "NM_001351543.2",
"protein_id": "NP_001338472.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 772,
"cds_start": -4,
"cds_end": null,
"cds_length": 2319,
"cdna_start": null,
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"cdna_length": 4212,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 20,
"intron_rank": 4,
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"gene_symbol": "TLE4",
"gene_hgnc_id": 11840,
"hgvs_c": "c.247-11659C>A",
"hgvs_p": null,
"transcript": "ENST00000706431.1",
"protein_id": "ENSP00000516378.1",
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"cds_start": -4,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 20,
"intron_rank": 4,
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"gene_symbol": "TLE4",
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"hgvs_c": "c.247-11659C>A",
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"transcript": "NM_001351546.2",
"protein_id": "NP_001338475.1",
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},
{
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],
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"gene_symbol": "TLE4",
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},
{
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],
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"gene_symbol": "TLE4",
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"hgvs_c": "c.252+24820C>A",
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"transcript": "NM_001351550.2",
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},
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],
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"gene_symbol": "TLE4",
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"hgvs_c": "c.252+24820C>A",
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},
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],
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},
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],
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"hgvs_c": "c.253-11659C>A",
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},
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],
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"gene_symbol": "TLE4",
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"hgvs_c": "c.253-11659C>A",
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"transcript": "ENST00000265284.10",
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],
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],
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"gene_symbol": "TLE4",
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"hgvs_c": "c.247-11659C>A",
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"transcript": "NM_001351563.2",
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},
{
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],
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"gene_symbol": "TLE4",
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"transcript": "NM_001351564.2",
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