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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: 12-43783707-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=43783707&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 43783707,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000613694.5",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.1171C>T",
"hgvs_p": "p.Arg391Cys",
"transcript": "NM_016123.4",
"protein_id": "NP_057207.2",
"transcript_support_level": null,
"aa_start": 391,
"aa_end": null,
"aa_length": 460,
"cds_start": 1171,
"cds_end": null,
"cds_length": 1383,
"cdna_start": 1246,
"cdna_end": null,
"cdna_length": 4284,
"mane_select": "ENST00000613694.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.1171C>T",
"hgvs_p": "p.Arg391Cys",
"transcript": "ENST00000613694.5",
"protein_id": "ENSP00000479889.3",
"transcript_support_level": 1,
"aa_start": 391,
"aa_end": null,
"aa_length": 460,
"cds_start": 1171,
"cds_end": null,
"cds_length": 1383,
"cdna_start": 1246,
"cdna_end": null,
"cdna_length": 4284,
"mane_select": "NM_016123.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.1171C>T",
"hgvs_p": "p.Arg391Cys",
"transcript": "ENST00000551736.5",
"protein_id": "ENSP00000446490.1",
"transcript_support_level": 1,
"aa_start": 391,
"aa_end": null,
"aa_length": 460,
"cds_start": 1171,
"cds_end": null,
"cds_length": 1383,
"cdna_start": 1284,
"cdna_end": null,
"cdna_length": 1684,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "n.*1073C>T",
"hgvs_p": null,
"transcript": "ENST00000547101.5",
"protein_id": "ENSP00000449317.1",
"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": 1703,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "n.*842C>T",
"hgvs_p": null,
"transcript": "ENST00000550615.5",
"protein_id": "ENSP00000449553.1",
"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": 1348,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "n.*1073C>T",
"hgvs_p": null,
"transcript": "ENST00000547101.5",
"protein_id": "ENSP00000449317.1",
"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": 1703,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "n.*842C>T",
"hgvs_p": null,
"transcript": "ENST00000550615.5",
"protein_id": "ENSP00000449553.1",
"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": 1348,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.1171C>T",
"hgvs_p": "p.Arg391Cys",
"transcript": "NM_001114182.3",
"protein_id": "NP_001107654.1",
"transcript_support_level": null,
"aa_start": 391,
"aa_end": null,
"aa_length": 460,
"cds_start": 1171,
"cds_end": null,
"cds_length": 1383,
"cdna_start": 1294,
"cdna_end": null,
"cdna_length": 4332,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.1171C>T",
"hgvs_p": "p.Arg391Cys",
"transcript": "NM_001351345.2",
"protein_id": "NP_001338274.1",
"transcript_support_level": null,
"aa_start": 391,
"aa_end": null,
"aa_length": 460,
"cds_start": 1171,
"cds_end": null,
"cds_length": 1383,
"cdna_start": 1478,
"cdna_end": null,
"cdna_length": 4516,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.799C>T",
"hgvs_p": "p.Arg267Cys",
"transcript": "NM_001145256.2",
"protein_id": "NP_001138728.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 336,
"cds_start": 799,
"cds_end": null,
"cds_length": 1011,
"cdna_start": 1148,
"cdna_end": null,
"cdna_length": 4186,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.799C>T",
"hgvs_p": "p.Arg267Cys",
"transcript": "NM_001145257.2",
"protein_id": "NP_001138729.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 336,
"cds_start": 799,
"cds_end": null,
"cds_length": 1011,
"cdna_start": 1100,
"cdna_end": null,
"cdna_length": 4138,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.799C>T",
"hgvs_p": "p.Arg267Cys",
"transcript": "NM_001145258.2",
"protein_id": "NP_001138730.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 336,
"cds_start": 799,
"cds_end": null,
"cds_length": 1011,
"cdna_start": 930,
"cdna_end": null,
"cdna_length": 3968,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.799C>T",
"hgvs_p": "p.Arg267Cys",
"transcript": "NM_001351338.2",
"protein_id": "NP_001338267.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 336,
"cds_start": 799,
"cds_end": null,
"cds_length": 1011,
"cdna_start": 1724,
"cdna_end": null,
"cdna_length": 4762,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.799C>T",
"hgvs_p": "p.Arg267Cys",
"transcript": "NM_001351339.2",
"protein_id": "NP_001338268.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 336,
"cds_start": 799,
"cds_end": null,
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"cdna_start": 1361,
"cdna_end": null,
"cdna_length": 4399,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.799C>T",
"hgvs_p": "p.Arg267Cys",
"transcript": "NM_001351340.2",
"protein_id": "NP_001338269.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 336,
"cds_start": 799,
"cds_end": null,
"cds_length": 1011,
"cdna_start": 1313,
"cdna_end": null,
"cdna_length": 4351,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.799C>T",
"hgvs_p": "p.Arg267Cys",
"transcript": "NM_001351341.2",
"protein_id": "NP_001338270.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 336,
"cds_start": 799,
"cds_end": null,
"cds_length": 1011,
"cdna_start": 1497,
"cdna_end": null,
"cdna_length": 4535,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.799C>T",
"hgvs_p": "p.Arg267Cys",
"transcript": "NM_001351342.2",
"protein_id": "NP_001338271.1",
"transcript_support_level": null,
"aa_start": 267,
"aa_end": null,
"aa_length": 336,
"cds_start": 799,
"cds_end": null,
"cds_length": 1011,
"cdna_start": 1143,
"cdna_end": null,
"cdna_length": 4181,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.799C>T",
"hgvs_p": "p.Arg267Cys",
"transcript": "ENST00000440781.6",
"protein_id": "ENSP00000408734.2",
"transcript_support_level": 2,
"aa_start": 267,
"aa_end": null,
"aa_length": 336,
"cds_start": 799,
"cds_end": null,
"cds_length": 1011,
"cdna_start": 937,
"cdna_end": null,
"cdna_length": 1409,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.562C>T",
"hgvs_p": "p.Arg188Cys",
"transcript": "NM_001351343.2",
"protein_id": "NP_001338272.1",
"transcript_support_level": null,
"aa_start": 188,
"aa_end": null,
"aa_length": 257,
"cds_start": 562,
"cds_end": null,
"cds_length": 774,
"cdna_start": 1198,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.562C>T",
"hgvs_p": "p.Arg188Cys",
"transcript": "NM_001351344.2",
"protein_id": "NP_001338273.1",
"transcript_support_level": null,
"aa_start": 188,
"aa_end": null,
"aa_length": 257,
"cds_start": 562,
"cds_end": null,
"cds_length": 774,
"cdna_start": 1014,
"cdna_end": null,
"cdna_length": 4052,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.1171C>T",
"hgvs_p": "p.Arg391Cys",
"transcript": "XM_005268943.4",
"protein_id": "XP_005269000.1",
"transcript_support_level": null,
"aa_start": 391,
"aa_end": null,
"aa_length": 460,
"cds_start": 1171,
"cds_end": null,
"cds_length": 1383,
"cdna_start": 1430,
"cdna_end": null,
"cdna_length": 4468,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.1171C>T",
"hgvs_p": "p.Arg391Cys",
"transcript": "XM_005268944.5",
"protein_id": "XP_005269001.1",
"transcript_support_level": null,
"aa_start": 391,
"aa_end": null,
"aa_length": 460,
"cds_start": 1171,
"cds_end": null,
"cds_length": 1383,
"cdna_start": 1960,
"cdna_end": null,
"cdna_length": 4998,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 12,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "IRAK4",
"gene_hgnc_id": 17967,
"hgvs_c": "c.1171C>T",
"hgvs_p": "p.Arg391Cys",
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}