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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: 9-121152028-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=121152028&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 121152028,
"ref": "A",
"alt": "G",
"effect": "intron_variant",
"transcript": "ENST00000373855.7",
"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": 44,
"intron_rank": 25,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.3964-457A>G",
"hgvs_p": null,
"transcript": "NM_007018.6",
"protein_id": "NP_008949.4",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2325,
"cds_start": -4,
"cds_end": null,
"cds_length": 6978,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7719,
"mane_select": "ENST00000373855.7",
"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": 44,
"intron_rank": 25,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.3964-457A>G",
"hgvs_p": null,
"transcript": "ENST00000373855.7",
"protein_id": "ENSP00000362962.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 2325,
"cds_start": -4,
"cds_end": null,
"cds_length": 6978,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7719,
"mane_select": "NM_007018.6",
"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": 32,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.3964-457A>G",
"hgvs_p": null,
"transcript": "ENST00000373847.6",
"protein_id": "ENSP00000362953.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1700,
"cds_start": -4,
"cds_end": null,
"cds_length": 5103,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5449,
"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": 33,
"intron_rank": 13,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.2314-457A>G",
"hgvs_p": null,
"transcript": "ENST00000686219.1",
"protein_id": "ENSP00000509692.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1806,
"cds_start": -4,
"cds_end": null,
"cds_length": 5421,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5665,
"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": 33,
"intron_rank": 13,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.2314-457A>G",
"hgvs_p": null,
"transcript": "ENST00000685839.1",
"protein_id": "ENSP00000509395.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1790,
"cds_start": -4,
"cds_end": null,
"cds_length": 5373,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5916,
"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": 33,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.2308-457A>G",
"hgvs_p": null,
"transcript": "NM_001330762.2",
"protein_id": "NP_001317691.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1773,
"cds_start": -4,
"cds_end": null,
"cds_length": 5322,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5934,
"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": 33,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.2308-457A>G",
"hgvs_p": null,
"transcript": "ENST00000373850.6",
"protein_id": "ENSP00000362956.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 1773,
"cds_start": -4,
"cds_end": null,
"cds_length": 5322,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5911,
"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": 32,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.2308-457A>G",
"hgvs_p": null,
"transcript": "NM_001369892.1",
"protein_id": "NP_001356821.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1726,
"cds_start": -4,
"cds_end": null,
"cds_length": 5181,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5793,
"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": 32,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.3964-457A>G",
"hgvs_p": null,
"transcript": "NM_001369893.1",
"protein_id": "NP_001356822.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1700,
"cds_start": -4,
"cds_end": null,
"cds_length": 5103,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5456,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": 25,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.4021-457A>G",
"hgvs_p": null,
"transcript": "NM_001369894.1",
"protein_id": "NP_001356823.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1610,
"cds_start": -4,
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"cdna_start": null,
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"cdna_length": 5462,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.3463-457A>G",
"hgvs_p": null,
"transcript": "NM_001369895.1",
"protein_id": "NP_001356824.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": -4,
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},
{
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"strand": true,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 6,
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"gene_symbol": "CNTRL",
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"hgvs_c": "n.765-457A>G",
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"transcript": "ENST00000431571.6",
"protein_id": "ENSP00000413014.2",
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},
{
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"strand": true,
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],
"exon_rank": null,
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"exon_count": 28,
"intron_rank": 14,
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"gene_symbol": "CNTRL",
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"hgvs_c": "n.2307+1545A>G",
"hgvs_p": null,
"transcript": "ENST00000687076.1",
"protein_id": "ENSP00000509694.1",
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},
{
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"strand": true,
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],
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"intron_rank": 24,
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"gene_symbol": "CNTRL",
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"hgvs_c": "n.6689-457A>G",
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},
{
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],
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"transcript": "ENST00000688832.1",
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},
{
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"strand": true,
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],
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"intron_rank": 24,
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"gene_symbol": "CNTRL",
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"hgvs_c": "n.*3476-457A>G",
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"transcript": "ENST00000689134.1",
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},
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],
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"gene_symbol": "CNTRL",
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"transcript": "ENST00000691066.1",
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},
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"strand": true,
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],
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"gene_symbol": "CNTRL",
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"hgvs_c": "n.2307+1545A>G",
"hgvs_p": null,
"transcript": "ENST00000692226.1",
"protein_id": "ENSP00000508636.1",
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"strand": true,
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],
"exon_rank": null,
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"exon_count": 31,
"intron_rank": 14,
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"gene_symbol": "CNTRL",
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"hgvs_c": "n.2307+1545A>G",
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},
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],
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},
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],
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"gene_symbol": "CNTRL",
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],
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"exon_count": 45,
"intron_rank": 25,
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"gene_symbol": "CNTRL",
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"hgvs_c": "c.4021-457A>G",
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"transcript": "XM_047422668.1",
"protein_id": "XP_047278624.1",
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"feature": null
},
{
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"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 45,
"intron_rank": 26,
"intron_rank_end": null,
"gene_symbol": "CNTRL",
"gene_hgnc_id": 1858,
"hgvs_c": "c.4021-457A>G",
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"transcript": "XM_047422669.1",
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},
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}