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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: 2-96602224-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=96602224&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 96602224,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001349256.2",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2374A>G",
"hgvs_p": "p.Thr792Ala",
"transcript": "NM_001115016.3",
"protein_id": "NP_001108488.1",
"transcript_support_level": null,
"aa_start": 792,
"aa_end": null,
"aa_length": 878,
"cds_start": 2374,
"cds_end": null,
"cds_length": 2637,
"cdna_start": 2454,
"cdna_end": null,
"cdna_length": 5156,
"mane_select": "ENST00000431828.6",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001115016.3"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2374A>G",
"hgvs_p": "p.Thr792Ala",
"transcript": "ENST00000431828.6",
"protein_id": "ENSP00000396749.1",
"transcript_support_level": 1,
"aa_start": 792,
"aa_end": null,
"aa_length": 878,
"cds_start": 2374,
"cds_end": null,
"cds_length": 2637,
"cdna_start": 2454,
"cdna_end": null,
"cdna_length": 5156,
"mane_select": "NM_001115016.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000431828.6"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "n.*2216A>G",
"hgvs_p": null,
"transcript": "ENST00000354204.10",
"protein_id": "ENSP00000346144.7",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5253,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000354204.10"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "n.*2216A>G",
"hgvs_p": null,
"transcript": "ENST00000354204.10",
"protein_id": "ENSP00000346144.7",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5253,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000354204.10"
},
{
"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": 21,
"intron_rank": 19,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "n.2338-448A>G",
"hgvs_p": null,
"transcript": "ENST00000420155.5",
"protein_id": "ENSP00000414426.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5028,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000420155.5"
},
{
"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": 20,
"intron_rank": 18,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "n.2344-448A>G",
"hgvs_p": null,
"transcript": "ENST00000487070.5",
"protein_id": null,
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": null,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4937,
"mane_select": null,
"mane_plus": null,
"biotype": "pseudogene",
"feature": "ENST00000487070.5"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2452A>G",
"hgvs_p": "p.Thr818Ala",
"transcript": "NM_001349256.2",
"protein_id": "NP_001336185.1",
"transcript_support_level": null,
"aa_start": 818,
"aa_end": null,
"aa_length": 907,
"cds_start": 2452,
"cds_end": null,
"cds_length": 2724,
"cdna_start": 2532,
"cdna_end": null,
"cdna_length": 3625,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349256.2"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2452A>G",
"hgvs_p": "p.Thr818Ala",
"transcript": "NM_001349257.2",
"protein_id": "NP_001336186.1",
"transcript_support_level": null,
"aa_start": 818,
"aa_end": null,
"aa_length": 904,
"cds_start": 2452,
"cds_end": null,
"cds_length": 2715,
"cdna_start": 2532,
"cdna_end": null,
"cdna_length": 5234,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349257.2"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2452A>G",
"hgvs_p": "p.Thr818Ala",
"transcript": "ENST00000666923.1",
"protein_id": "ENSP00000499674.1",
"transcript_support_level": null,
"aa_start": 818,
"aa_end": null,
"aa_length": 904,
"cds_start": 2452,
"cds_end": null,
"cds_length": 2715,
"cdna_start": 2536,
"cdna_end": null,
"cdna_length": 5226,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000666923.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2452A>G",
"hgvs_p": "p.Thr818Ala",
"transcript": "ENST00000883013.1",
"protein_id": "ENSP00000553072.1",
"transcript_support_level": null,
"aa_start": 818,
"aa_end": null,
"aa_length": 904,
"cds_start": 2452,
"cds_end": null,
"cds_length": 2715,
"cdna_start": 2613,
"cdna_end": null,
"cdna_length": 5315,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883013.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2452A>G",
"hgvs_p": "p.Thr818Ala",
"transcript": "ENST00000948575.1",
"protein_id": "ENSP00000618634.1",
"transcript_support_level": null,
"aa_start": 818,
"aa_end": null,
"aa_length": 904,
"cds_start": 2452,
"cds_end": null,
"cds_length": 2715,
"cdna_start": 2635,
"cdna_end": null,
"cdna_length": 5335,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948575.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2446A>G",
"hgvs_p": "p.Thr816Ala",
"transcript": "NM_001349258.2",
"protein_id": "NP_001336187.1",
"transcript_support_level": null,
"aa_start": 816,
"aa_end": null,
"aa_length": 902,
"cds_start": 2446,
"cds_end": null,
"cds_length": 2709,
"cdna_start": 2526,
"cdna_end": null,
"cdna_length": 5228,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001349258.2"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2446A>G",
"hgvs_p": "p.Thr816Ala",
"transcript": "ENST00000883015.1",
"protein_id": "ENSP00000553074.1",
"transcript_support_level": null,
"aa_start": 816,
"aa_end": null,
"aa_length": 902,
"cds_start": 2446,
"cds_end": null,
"cds_length": 2709,
"cdna_start": 2571,
"cdna_end": null,
"cdna_length": 5275,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883015.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 20,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2446A>G",
"hgvs_p": "p.Thr816Ala",
"transcript": "ENST00000948573.1",
"protein_id": "ENSP00000618632.1",
"transcript_support_level": null,
"aa_start": 816,
"aa_end": null,
"aa_length": 902,
"cds_start": 2446,
"cds_end": null,
"cds_length": 2709,
"cdna_start": 2523,
"cdna_end": null,
"cdna_length": 5195,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948573.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2374A>G",
"hgvs_p": "p.Thr792Ala",
"transcript": "ENST00000883014.1",
"protein_id": "ENSP00000553073.1",
"transcript_support_level": null,
"aa_start": 792,
"aa_end": null,
"aa_length": 878,
"cds_start": 2374,
"cds_end": null,
"cds_length": 2637,
"cdna_start": 2504,
"cdna_end": null,
"cdna_length": 5207,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883014.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2374A>G",
"hgvs_p": "p.Thr792Ala",
"transcript": "ENST00000948574.1",
"protein_id": "ENSP00000618633.1",
"transcript_support_level": null,
"aa_start": 792,
"aa_end": null,
"aa_length": 878,
"cds_start": 2374,
"cds_end": null,
"cds_length": 2637,
"cdna_start": 2608,
"cdna_end": null,
"cdna_length": 5280,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948574.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2374A>G",
"hgvs_p": "p.Thr792Ala",
"transcript": "ENST00000948576.1",
"protein_id": "ENSP00000618635.1",
"transcript_support_level": null,
"aa_start": 792,
"aa_end": null,
"aa_length": 878,
"cds_start": 2374,
"cds_end": null,
"cds_length": 2637,
"cdna_start": 2531,
"cdna_end": null,
"cdna_length": 5223,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948576.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 18,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2374A>G",
"hgvs_p": "p.Thr792Ala",
"transcript": "ENST00000948577.1",
"protein_id": "ENSP00000618636.1",
"transcript_support_level": null,
"aa_start": 792,
"aa_end": null,
"aa_length": 878,
"cds_start": 2374,
"cds_end": null,
"cds_length": 2637,
"cdna_start": 2608,
"cdna_end": null,
"cdna_length": 3813,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948577.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2368A>G",
"hgvs_p": "p.Thr790Ala",
"transcript": "ENST00000883008.1",
"protein_id": "ENSP00000553067.1",
"transcript_support_level": null,
"aa_start": 790,
"aa_end": null,
"aa_length": 876,
"cds_start": 2368,
"cds_end": null,
"cds_length": 2631,
"cdna_start": 2510,
"cdna_end": null,
"cdna_length": 5212,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883008.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2359A>G",
"hgvs_p": "p.Thr787Ala",
"transcript": "ENST00000883011.1",
"protein_id": "ENSP00000553070.1",
"transcript_support_level": null,
"aa_start": 787,
"aa_end": null,
"aa_length": 873,
"cds_start": 2359,
"cds_end": null,
"cds_length": 2622,
"cdna_start": 2459,
"cdna_end": null,
"cdna_length": 5149,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000883011.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2353A>G",
"hgvs_p": "p.Thr785Ala",
"transcript": "ENST00000948571.1",
"protein_id": "ENSP00000618630.1",
"transcript_support_level": null,
"aa_start": 785,
"aa_end": null,
"aa_length": 871,
"cds_start": 2353,
"cds_end": null,
"cds_length": 2616,
"cdna_start": 2433,
"cdna_end": null,
"cdna_length": 5105,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000948571.1"
},
{
"aa_ref": "T",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 19,
"exon_rank_end": null,
"exon_count": 21,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KANSL3",
"gene_hgnc_id": 25473,
"hgvs_c": "c.2341A>G",
"hgvs_p": "p.Thr781Ala",
"transcript": "ENST00000883009.1",
"protein_id": "ENSP00000553068.1",
"transcript_support_level": null,
"aa_start": 781,
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"phenotype_combined": "not specified",
"pathogenicity_classification_combined": "Uncertain significance",
"custom_annotations": null
}
],
"message": null
}