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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: 2-179501964-T-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=179501964&ref=T&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 179501964,
"ref": "T",
"alt": "A",
"effect": "intron_variant",
"transcript": "ENST00000410066.7",
"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": 10,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "ZNF385B",
"gene_hgnc_id": 26332,
"hgvs_c": "c.552+16564A>T",
"hgvs_p": null,
"transcript": "NM_152520.6",
"protein_id": "NP_689733.4",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 486,
"cds_start": -4,
"cds_end": null,
"cds_length": 1461,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3395,
"mane_select": "ENST00000410066.7",
"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": 10,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "ZNF385B",
"gene_hgnc_id": 26332,
"hgvs_c": "c.552+16564A>T",
"hgvs_p": null,
"transcript": "ENST00000410066.7",
"protein_id": "ENSP00000386845.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 486,
"cds_start": -4,
"cds_end": null,
"cds_length": 1461,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3395,
"mane_select": "NM_152520.6",
"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": 13,
"intron_rank": 7,
"intron_rank_end": null,
"gene_symbol": "ZNF385B",
"gene_hgnc_id": 26332,
"hgvs_c": "n.781+12121A>T",
"hgvs_p": null,
"transcript": "ENST00000466398.5",
"protein_id": null,
"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": 1901,
"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": 11,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "ZNF385B",
"gene_hgnc_id": 26332,
"hgvs_c": "c.690+16564A>T",
"hgvs_p": null,
"transcript": "NM_001352809.2",
"protein_id": "NP_001339738.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 532,
"cds_start": -4,
"cds_end": null,
"cds_length": 1599,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3533,
"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": 11,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "ZNF385B",
"gene_hgnc_id": 26332,
"hgvs_c": "c.552+16564A>T",
"hgvs_p": null,
"transcript": "NM_001352810.2",
"protein_id": "NP_001339739.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 513,
"cds_start": -4,
"cds_end": null,
"cds_length": 1542,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3476,
"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": 11,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "ZNF385B",
"gene_hgnc_id": 26332,
"hgvs_c": "c.591+16564A>T",
"hgvs_p": null,
"transcript": "NM_001352811.2",
"protein_id": "NP_001339740.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 499,
"cds_start": -4,
"cds_end": null,
"cds_length": 1500,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3434,
"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": 11,
"intron_rank": 6,
"intron_rank_end": null,
"gene_symbol": "ZNF385B",
"gene_hgnc_id": 26332,
"hgvs_c": "c.552+16564A>T",
"hgvs_p": null,
"transcript": "NM_001352808.2",
"protein_id": "NP_001339737.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 486,
"cds_start": -4,
"cds_end": null,
"cds_length": 1461,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3481,
"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": 9,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "ZNF385B",
"gene_hgnc_id": 26332,
"hgvs_c": "c.303+16564A>T",
"hgvs_p": null,
"transcript": "NM_001352812.2",
"protein_id": "NP_001339741.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 403,
"cds_start": -4,
"cds_end": null,
"cds_length": 1212,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2588,
"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": 3,
"intron_rank_end": null,
"gene_symbol": "ZNF385B",
"gene_hgnc_id": 26332,
"hgvs_c": "c.279+16564A>T",
"hgvs_p": null,
"transcript": "NM_001113397.2",
"protein_id": "NP_001106868.1",
"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": 3229,
"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": 8,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "ZNF385B",
"gene_hgnc_id": 26332,
"hgvs_c": "c.279+16564A>T",
"hgvs_p": null,
"transcript": "ENST00000409343.5",
"protein_id": "ENSP00000386379.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 395,
"cds_start": -4,
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"cdna_start": null,
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"mane_select": null,
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"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": 8,
"intron_rank": 3,
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"gene_symbol": "ZNF385B",
"gene_hgnc_id": 26332,
"hgvs_c": "c.201+16564A>T",
"hgvs_p": null,
"transcript": "NM_001113398.3",
"protein_id": "NP_001106869.1",
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},
{
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"strand": false,
"consequences": [
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],
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"gene_symbol": "ZNF385B",
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"hgvs_c": "c.201+16564A>T",
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"transcript": "NM_001282725.3",
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},
{
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],
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"gene_symbol": "ZNF385B",
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"hgvs_c": "c.201+16564A>T",
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"transcript": "NM_001352813.2",
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},
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],
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"gene_symbol": "ZNF385B",
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"hgvs_c": "c.201+16564A>T",
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},
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],
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},
{
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],
"exon_rank": null,
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"gene_symbol": "ZNF385B",
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"hgvs_c": "c.201+16564A>T",
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],
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"gene_symbol": "ZNF385B",
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"hgvs_c": "c.201+16564A>T",
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},
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],
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"gene_symbol": "ZNF385B",
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"hgvs_c": "c.165+16564A>T",
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},
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],
"exon_rank": null,
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"gene_symbol": "ZNF385B",
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"hgvs_c": "c.111+16564A>T",
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"gene_symbol": "ZNF385B",
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],
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},
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],
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"gene_symbol": "ZNF385B",
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"hgvs_c": "n.476+16564A>T",
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"transcript": "ENST00000469551.5",
"protein_id": null,
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},
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 2,
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"gene_symbol": "ZNF385B",
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}