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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: 2-26280101-A-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=26280101&ref=A&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 26280101,
"ref": "A",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_000183.3",
"consequences": [
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "NM_000183.3",
"protein_id": "NP_000174.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 979,
"cdna_end": null,
"cdna_length": 1997,
"mane_select": "ENST00000317799.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000183.3"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000317799.10",
"protein_id": "ENSP00000325136.5",
"transcript_support_level": 1,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 979,
"cdna_end": null,
"cdna_length": 1997,
"mane_select": "NM_000183.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000317799.10"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.1003A>T",
"hgvs_p": "p.Asn335Tyr",
"transcript": "ENST00000942431.1",
"protein_id": "ENSP00000612490.1",
"transcript_support_level": null,
"aa_start": 335,
"aa_end": null,
"aa_length": 502,
"cds_start": 1003,
"cds_end": null,
"cds_length": 1509,
"cdna_start": 1079,
"cdna_end": null,
"cdna_length": 2096,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942431.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.949A>T",
"hgvs_p": "p.Asn317Tyr",
"transcript": "ENST00000942426.1",
"protein_id": "ENSP00000612485.1",
"transcript_support_level": null,
"aa_start": 317,
"aa_end": null,
"aa_length": 484,
"cds_start": 949,
"cds_end": null,
"cds_length": 1455,
"cdna_start": 1163,
"cdna_end": null,
"cdna_length": 2177,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942426.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.946A>T",
"hgvs_p": "p.Asn316Tyr",
"transcript": "ENST00000859601.1",
"protein_id": "ENSP00000529660.1",
"transcript_support_level": null,
"aa_start": 316,
"aa_end": null,
"aa_length": 483,
"cds_start": 946,
"cds_end": null,
"cds_length": 1452,
"cdna_start": 979,
"cdna_end": null,
"cdna_length": 1630,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000859601.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.931A>T",
"hgvs_p": "p.Asn311Tyr",
"transcript": "ENST00000942427.1",
"protein_id": "ENSP00000612486.1",
"transcript_support_level": null,
"aa_start": 311,
"aa_end": null,
"aa_length": 478,
"cds_start": 931,
"cds_end": null,
"cds_length": 1437,
"cdna_start": 1017,
"cdna_end": null,
"cdna_length": 2034,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942427.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000859582.1",
"protein_id": "ENSP00000529641.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 1067,
"cdna_end": null,
"cdna_length": 2082,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000859582.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000859593.1",
"protein_id": "ENSP00000529652.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 999,
"cdna_end": null,
"cdna_length": 2017,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000859593.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000859599.1",
"protein_id": "ENSP00000529658.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 998,
"cdna_end": null,
"cdna_length": 1651,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000859599.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000942424.1",
"protein_id": "ENSP00000612483.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 1227,
"cdna_end": null,
"cdna_length": 2244,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942424.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000942425.1",
"protein_id": "ENSP00000612484.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 1309,
"cdna_end": null,
"cdna_length": 2324,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942425.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000942434.1",
"protein_id": "ENSP00000612493.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 1005,
"cdna_end": null,
"cdna_length": 2023,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942434.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 17,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000942437.1",
"protein_id": "ENSP00000612496.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 1023,
"cdna_end": null,
"cdna_length": 2040,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942437.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000942440.1",
"protein_id": "ENSP00000612499.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 1042,
"cdna_end": null,
"cdna_length": 2059,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942440.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000942441.1",
"protein_id": "ENSP00000612500.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 1025,
"cdna_end": null,
"cdna_length": 2039,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942441.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000942445.1",
"protein_id": "ENSP00000612504.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 474,
"cds_start": 919,
"cds_end": null,
"cds_length": 1425,
"cdna_start": 1040,
"cdna_end": null,
"cdna_length": 2057,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942445.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.913A>T",
"hgvs_p": "p.Asn305Tyr",
"transcript": "ENST00000859584.1",
"protein_id": "ENSP00000529643.1",
"transcript_support_level": null,
"aa_start": 305,
"aa_end": null,
"aa_length": 472,
"cds_start": 913,
"cds_end": null,
"cds_length": 1419,
"cdna_start": 999,
"cdna_end": null,
"cdna_length": 2017,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000859584.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.919A>T",
"hgvs_p": "p.Asn307Tyr",
"transcript": "ENST00000859587.1",
"protein_id": "ENSP00000529646.1",
"transcript_support_level": null,
"aa_start": 307,
"aa_end": null,
"aa_length": 472,
"cds_start": 919,
"cds_end": null,
"cds_length": 1419,
"cdna_start": 990,
"cdna_end": null,
"cdna_length": 2002,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000859587.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.907A>T",
"hgvs_p": "p.Asn303Tyr",
"transcript": "ENST00000942429.1",
"protein_id": "ENSP00000612488.1",
"transcript_support_level": null,
"aa_start": 303,
"aa_end": null,
"aa_length": 470,
"cds_start": 907,
"cds_end": null,
"cds_length": 1413,
"cdna_start": 984,
"cdna_end": null,
"cdna_length": 2002,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942429.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.901A>T",
"hgvs_p": "p.Asn301Tyr",
"transcript": "ENST00000859600.1",
"protein_id": "ENSP00000529659.1",
"transcript_support_level": null,
"aa_start": 301,
"aa_end": null,
"aa_length": 468,
"cds_start": 901,
"cds_end": null,
"cds_length": 1407,
"cdna_start": 957,
"cdna_end": null,
"cdna_length": 1606,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000859600.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.898A>T",
"hgvs_p": "p.Asn300Tyr",
"transcript": "ENST00000942435.1",
"protein_id": "ENSP00000612494.1",
"transcript_support_level": null,
"aa_start": 300,
"aa_end": null,
"aa_length": 467,
"cds_start": 898,
"cds_end": null,
"cds_length": 1404,
"cdna_start": 958,
"cdna_end": null,
"cdna_length": 1973,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942435.1"
},
{
"aa_ref": "N",
"aa_alt": "Y",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "HADHB",
"gene_hgnc_id": 4803,
"hgvs_c": "c.874A>T",
"hgvs_p": "p.Asn292Tyr",
"transcript": "NM_001281512.2",
"protein_id": "NP_001268441.1",
"transcript_support_level": null,
"aa_start": 292,
"aa_end": null,
"aa_length": 459,
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"clinvar_disease": "",
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}
],
"message": null
}