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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: 17-74773195-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=17&pos=74773195&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "17",
"pos": 74773195,
"ref": "T",
"alt": "C",
"effect": "intron_variant",
"transcript": "ENST00000357814.8",
"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": 7,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "c.191-156A>G",
"hgvs_p": null,
"transcript": "NM_015654.5",
"protein_id": "NP_056469.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 207,
"cds_start": -4,
"cds_end": null,
"cds_length": 624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1907,
"mane_select": "ENST00000357814.8",
"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": 7,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "c.191-156A>G",
"hgvs_p": null,
"transcript": "ENST00000357814.8",
"protein_id": "ENSP00000350467.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 207,
"cds_start": -4,
"cds_end": null,
"cds_length": 624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1907,
"mane_select": "NM_015654.5",
"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": 7,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "c.188-156A>G",
"hgvs_p": null,
"transcript": "ENST00000580301.5",
"protein_id": "ENSP00000462019.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 206,
"cds_start": -4,
"cds_end": null,
"cds_length": 621,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1860,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 3,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "n.662A>G",
"hgvs_p": null,
"transcript": "ENST00000582168.5",
"protein_id": null,
"transcript_support_level": 2,
"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": 863,
"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": 7,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "c.206-156A>G",
"hgvs_p": null,
"transcript": "NM_001305082.2",
"protein_id": "NP_001292011.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 212,
"cds_start": -4,
"cds_end": null,
"cds_length": 639,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2052,
"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": 7,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "c.206-156A>G",
"hgvs_p": null,
"transcript": "ENST00000578822.5",
"protein_id": "ENSP00000462835.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 212,
"cds_start": -4,
"cds_end": null,
"cds_length": 639,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 839,
"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": 7,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "c.203-156A>G",
"hgvs_p": null,
"transcript": "ENST00000582870.5",
"protein_id": "ENSP00000464281.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 211,
"cds_start": -4,
"cds_end": null,
"cds_length": 636,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 896,
"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": 7,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "c.191-156A>G",
"hgvs_p": null,
"transcript": "NM_001305078.2",
"protein_id": "NP_001292007.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 207,
"cds_start": -4,
"cds_end": null,
"cds_length": 624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1903,
"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": 5,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "c.188-156A>G",
"hgvs_p": null,
"transcript": "ENST00000580632.5",
"protein_id": "ENSP00000463523.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 207,
"cds_start": -4,
"cds_end": null,
"cds_length": 624,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 799,
"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": 7,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "c.188-156A>G",
"hgvs_p": null,
"transcript": "NM_001305077.2",
"protein_id": "NP_001292006.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 206,
"cds_start": -4,
"cds_end": null,
"cds_length": 621,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1904,
"mane_select": null,
"mane_plus": null,
"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": 7,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "c.188-156A>G",
"hgvs_p": null,
"transcript": "NM_001305081.2",
"protein_id": "NP_001292010.1",
"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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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 7,
"intron_rank": 3,
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"gene_symbol": "NAT9",
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"hgvs_c": "c.191-156A>G",
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"transcript": "NM_001305080.2",
"protein_id": "NP_001292009.1",
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 7,
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"gene_symbol": "NAT9",
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"hgvs_c": "c.191-156A>G",
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"transcript": "ENST00000581136.5",
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},
{
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],
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"gene_symbol": "NAT9",
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"hgvs_c": "c.188-156A>G",
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"transcript": "NM_001305083.2",
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},
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],
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"gene_symbol": "NAT9",
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"transcript": "ENST00000579218.5",
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 6,
"intron_rank": 3,
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"gene_symbol": "NAT9",
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"hgvs_c": "c.188-156A>G",
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"transcript": "NM_001305086.2",
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},
{
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],
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"hgvs_c": "c.191-156A>G",
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"transcript": "NM_001305084.3",
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},
{
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],
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"exon_count": 6,
"intron_rank": 3,
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"gene_symbol": "NAT9",
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"hgvs_c": "c.191-156A>G",
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"transcript": "ENST00000582524.5",
"protein_id": "ENSP00000462120.1",
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},
{
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"strand": false,
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],
"exon_rank": null,
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"exon_count": 6,
"intron_rank": 3,
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"gene_symbol": "NAT9",
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"hgvs_c": "c.188-156A>G",
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"transcript": "NM_001305085.3",
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],
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},
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],
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"gene_symbol": "NAT9",
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},
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],
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"gene_symbol": "NAT9",
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"hgvs_c": "c.191-156A>G",
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"transcript": "ENST00000583476.5",
"protein_id": "ENSP00000463353.1",
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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,
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"exon_count": 6,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "NAT9",
"gene_hgnc_id": 23133,
"hgvs_c": "c.116-156A>G",
"hgvs_p": null,
"transcript": "NM_001305087.3",
"protein_id": "NP_001292016.1",
"transcript_support_level": null,
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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}