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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: 17-16101873-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=16101873&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 16101873,
"ref": "T",
"alt": "A",
"effect": "intron_variant",
"transcript": "NM_001439111.1",
"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": 46,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2183-116A>T",
"hgvs_p": null,
"transcript": "NM_006311.4",
"protein_id": "NP_006302.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2440,
"cds_start": null,
"cds_end": null,
"cds_length": 7323,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000268712.8",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_006311.4"
},
{
"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": 46,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2183-116A>T",
"hgvs_p": null,
"transcript": "ENST00000268712.8",
"protein_id": "ENSP00000268712.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2440,
"cds_start": null,
"cds_end": null,
"cds_length": 7323,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_006311.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000268712.8"
},
{
"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": 47,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2183-68A>T",
"hgvs_p": null,
"transcript": "ENST00000436068.2",
"protein_id": "ENSP00000389839.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2514,
"cds_start": null,
"cds_end": null,
"cds_length": 7545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000436068.2"
},
{
"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": 45,
"intron_rank": 18,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2183-68A>T",
"hgvs_p": null,
"transcript": "ENST00000395851.5",
"protein_id": "ENSP00000379192.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2337,
"cds_start": null,
"cds_end": null,
"cds_length": 7014,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000395851.5"
},
{
"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": 19,
"intron_rank": 16,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.1856-68A>T",
"hgvs_p": null,
"transcript": "ENST00000395848.5",
"protein_id": "ENSP00000379189.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 914,
"cds_start": null,
"cds_end": null,
"cds_length": 2745,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000395848.5"
},
{
"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": 49,
"intron_rank": 21,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2213-68A>T",
"hgvs_p": null,
"transcript": "ENST00000917643.1",
"protein_id": "ENSP00000587702.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2524,
"cds_start": null,
"cds_end": null,
"cds_length": 7575,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917643.1"
},
{
"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": 48,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2210-68A>T",
"hgvs_p": null,
"transcript": "ENST00000917649.1",
"protein_id": "ENSP00000587708.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2523,
"cds_start": null,
"cds_end": null,
"cds_length": 7572,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917649.1"
},
{
"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": 47,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2183-68A>T",
"hgvs_p": null,
"transcript": "NM_001439111.1",
"protein_id": "NP_001426040.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2514,
"cds_start": null,
"cds_end": null,
"cds_length": 7545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001439111.1"
},
{
"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": 47,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2183-68A>T",
"hgvs_p": null,
"transcript": "ENST00000704744.1",
"protein_id": "ENSP00000516021.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2514,
"cds_start": null,
"cds_end": null,
"cds_length": 7545,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000704744.1"
},
{
"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": 48,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2210-116A>T",
"hgvs_p": null,
"transcript": "ENST00000917655.1",
"protein_id": "ENSP00000587714.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2507,
"cds_start": null,
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"cds_length": 7524,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000917655.1"
},
{
"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": 46,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2183-68A>T",
"hgvs_p": null,
"transcript": "ENST00000917645.1",
"protein_id": "ENSP00000587704.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2471,
"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "ENST00000917645.1"
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 48,
"intron_rank": 21,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2213-68A>T",
"hgvs_p": null,
"transcript": "NM_001439112.1",
"protein_id": "NP_001426041.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "NM_001439112.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 47,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
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"hgvs_c": "c.2213-68A>T",
"hgvs_p": null,
"transcript": "ENST00000704745.1",
"protein_id": "ENSP00000516022.1",
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"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "ENST00000704745.1"
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 48,
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"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2213-68A>T",
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"biotype": "protein_coding",
"feature": "ENST00000917656.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 47,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2210-68A>T",
"hgvs_p": null,
"transcript": "ENST00000917644.1",
"protein_id": "ENSP00000587703.1",
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"cdna_start": null,
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"feature": "ENST00000917644.1"
},
{
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"protein_coding": true,
"strand": false,
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],
"exon_rank": null,
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"intron_rank": 20,
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"gene_symbol": "NCOR1",
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"hgvs_c": "c.2210-68A>T",
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"transcript": "ENST00000917650.1",
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},
{
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"strand": false,
"consequences": [
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],
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"intron_rank": 20,
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"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2210-68A>T",
"hgvs_p": null,
"transcript": "NM_001439113.1",
"protein_id": "NP_001426042.1",
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"biotype": "protein_coding",
"feature": "NM_001439113.1"
},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2207-68A>T",
"hgvs_p": null,
"transcript": "ENST00000917654.1",
"protein_id": "ENSP00000587713.1",
"transcript_support_level": null,
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},
{
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"strand": false,
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],
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"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2186-68A>T",
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},
{
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"consequences": [
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],
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"gene_symbol": "NCOR1",
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"transcript": "ENST00000917647.1",
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},
{
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"consequences": [
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],
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"gene_symbol": "NCOR1",
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"hgvs_c": "c.2183-68A>T",
"hgvs_p": null,
"transcript": "NM_001439115.1",
"protein_id": "NP_001426044.1",
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "NM_001439115.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 46,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "NCOR1",
"gene_hgnc_id": 7672,
"hgvs_c": "c.2183-68A>T",
"hgvs_p": null,
"transcript": "ENST00000917651.1",
"protein_id": "ENSP00000587710.1",
"transcript_support_level": null,
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"mane_select": null,
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"biotype": "protein_coding",
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},
{
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"protein_coding": true,
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"consequences": [
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],
"exon_rank": null,
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}