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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: 3-21448956-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=21448956&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 21448956,
"ref": "T",
"alt": "G",
"effect": "intron_variant",
"transcript": "ENST00000281523.8",
"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": 8,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "ZNF385D",
"gene_hgnc_id": 26191,
"hgvs_c": "c.440-11753A>C",
"hgvs_p": null,
"transcript": "NM_024697.3",
"protein_id": "NP_078973.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 395,
"cds_start": -4,
"cds_end": null,
"cds_length": 1188,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10478,
"mane_select": "ENST00000281523.8",
"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": 8,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "ZNF385D",
"gene_hgnc_id": 26191,
"hgvs_c": "c.440-11753A>C",
"hgvs_p": null,
"transcript": "ENST00000281523.8",
"protein_id": "ENSP00000281523.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 395,
"cds_start": -4,
"cds_end": null,
"cds_length": 1188,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10478,
"mane_select": "NM_024697.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "ZNF385D",
"gene_hgnc_id": 26191,
"hgvs_c": "n.*367+10376A>C",
"hgvs_p": null,
"transcript": "ENST00000494118.5",
"protein_id": "ENSP00000493727.1",
"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": 1050,
"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": 10,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "ZNF385D",
"gene_hgnc_id": 26191,
"hgvs_c": "c.743-7214A>C",
"hgvs_p": null,
"transcript": "ENST00000706131.1",
"protein_id": "ENSP00000516216.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 515,
"cds_start": -4,
"cds_end": null,
"cds_length": 1548,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4424,
"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": 10,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "ZNF385D",
"gene_hgnc_id": 26191,
"hgvs_c": "c.743-11753A>C",
"hgvs_p": null,
"transcript": "ENST00000494108.3",
"protein_id": "ENSP00000495609.3",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 496,
"cds_start": -4,
"cds_end": null,
"cds_length": 1491,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4707,
"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": 8,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "ZNF385D",
"gene_hgnc_id": 26191,
"hgvs_c": "c.431-11753A>C",
"hgvs_p": null,
"transcript": "ENST00000706134.1",
"protein_id": "ENSP00000516219.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 392,
"cds_start": -4,
"cds_end": null,
"cds_length": 1179,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1549,
"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": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ZNF385D",
"gene_hgnc_id": 26191,
"hgvs_c": "c.125-7214A>C",
"hgvs_p": null,
"transcript": "ENST00000495739.1",
"protein_id": "ENSP00000498106.1",
"transcript_support_level": 3,
"aa_start": null,
"aa_end": null,
"aa_length": 156,
"cds_start": -4,
"cds_end": null,
"cds_length": 471,
"cdna_start": null,
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"cdna_length": 567,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "ZNF385D",
"gene_hgnc_id": 26191,
"hgvs_c": "n.*264-11753A>C",
"hgvs_p": null,
"transcript": "ENST00000446749.2",
"protein_id": "ENSP00000388232.1",
"transcript_support_level": 5,
"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": 1586,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "ZNF385D",
"gene_hgnc_id": 26191,
"hgvs_c": "n.*171-11753A>C",
"hgvs_p": null,
"transcript": "ENST00000706132.1",
"protein_id": "ENSP00000516217.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
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"cdna_length": 1622,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
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"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 12,
"intron_rank": 8,
"intron_rank_end": null,
"gene_symbol": "ZNF385D",
"gene_hgnc_id": 26191,
"hgvs_c": "n.*635+10376A>C",
"hgvs_p": null,
"transcript": "ENST00000706133.1",
"protein_id": "ENSP00000516218.1",
"transcript_support_level": null,
"aa_start": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 9,
"intron_rank": 6,
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"gene_symbol": "ZNF385D",
"gene_hgnc_id": 26191,
"hgvs_c": "n.*339-5638A>C",
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"transcript": "ENST00000706135.1",
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},
{
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"strand": false,
"consequences": [
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],
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},
{
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],
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"gene_symbol": "ZNF385D",
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},
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],
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"gene_symbol": "ZNF385D",
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"hgvs_c": "c.743-7214A>C",
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},
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],
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},
{
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],
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"gene_symbol": "ZNF385D",
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},
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],
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"gene_symbol": "ZNF385D",
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"hgvs_c": "c.485-7214A>C",
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],
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},
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],
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"gene_symbol": "ZNF385D",
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"transcript": "XM_047448958.1",
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},
{
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"consequences": [
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],
"exon_rank": null,
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"exon_count": 8,
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"gene_symbol": "ZNF385D",
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"hgvs_c": "c.431-11753A>C",
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"transcript": "XM_047448959.1",
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}