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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: 10-242118-T-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=242118&ref=T&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "10",
"pos": 242118,
"ref": "T",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000381604.9",
"consequences": [
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "NM_001370100.5",
"protein_id": "NP_001357029.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 602,
"cds_start": 929,
"cds_end": null,
"cds_length": 1809,
"cdna_start": 1053,
"cdna_end": null,
"cdna_length": 4100,
"mane_select": "ENST00000381604.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "ENST00000381604.9",
"protein_id": "ENSP00000371017.6",
"transcript_support_level": 5,
"aa_start": 310,
"aa_end": null,
"aa_length": 602,
"cds_start": 929,
"cds_end": null,
"cds_length": 1809,
"cdna_start": 1053,
"cdna_end": null,
"cdna_length": 4100,
"mane_select": "NM_001370100.5",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "ENST00000397962.8",
"protein_id": "ENSP00000381053.3",
"transcript_support_level": 1,
"aa_start": 310,
"aa_end": null,
"aa_length": 602,
"cds_start": 929,
"cds_end": null,
"cds_length": 1809,
"cdna_start": 1270,
"cdna_end": null,
"cdna_length": 2150,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "ENST00000558098.4",
"protein_id": "ENSP00000452959.1",
"transcript_support_level": 1,
"aa_start": 310,
"aa_end": null,
"aa_length": 568,
"cds_start": 929,
"cds_end": null,
"cds_length": 1707,
"cdna_start": 929,
"cdna_end": null,
"cdna_length": 1859,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.926T>G",
"hgvs_p": "p.Phe309Cys",
"transcript": "ENST00000509513.6",
"protein_id": "ENSP00000424205.2",
"transcript_support_level": 1,
"aa_start": 309,
"aa_end": null,
"aa_length": 567,
"cds_start": 926,
"cds_end": null,
"cds_length": 1704,
"cdna_start": 1135,
"cdna_end": null,
"cdna_length": 2065,
"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": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "n.*871T>G",
"hgvs_p": null,
"transcript": "ENST00000381584.6",
"protein_id": "ENSP00000370996.2",
"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": 4157,
"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": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "n.*871T>G",
"hgvs_p": null,
"transcript": "ENST00000381584.6",
"protein_id": "ENSP00000370996.2",
"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": 4157,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.974T>G",
"hgvs_p": "p.Phe325Cys",
"transcript": "ENST00000397955.7",
"protein_id": "ENSP00000381046.3",
"transcript_support_level": 5,
"aa_start": 325,
"aa_end": null,
"aa_length": 617,
"cds_start": 974,
"cds_end": null,
"cds_length": 1854,
"cdna_start": 1034,
"cdna_end": null,
"cdna_length": 3961,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "NM_001370097.3",
"protein_id": "NP_001357026.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 602,
"cds_start": 929,
"cds_end": null,
"cds_length": 1809,
"cdna_start": 1041,
"cdna_end": null,
"cdna_length": 4085,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "NM_001370098.2",
"protein_id": "NP_001357027.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 602,
"cds_start": 929,
"cds_end": null,
"cds_length": 1809,
"cdna_start": 1352,
"cdna_end": null,
"cdna_length": 4396,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "NM_001370099.2",
"protein_id": "NP_001357028.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 602,
"cds_start": 929,
"cds_end": null,
"cds_length": 1809,
"cdna_start": 986,
"cdna_end": null,
"cdna_length": 4030,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "NM_001370101.2",
"protein_id": "NP_001357030.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 602,
"cds_start": 929,
"cds_end": null,
"cds_length": 1809,
"cdna_start": 1023,
"cdna_end": null,
"cdna_length": 4067,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "NM_001370102.2",
"protein_id": "NP_001357031.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 602,
"cds_start": 929,
"cds_end": null,
"cds_length": 1809,
"cdna_start": 1557,
"cdna_end": null,
"cdna_length": 4601,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "NM_006624.7",
"protein_id": "NP_006615.2",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 602,
"cds_start": 929,
"cds_end": null,
"cds_length": 1809,
"cdna_start": 1251,
"cdna_end": null,
"cdna_length": 4295,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "ENST00000381591.5",
"protein_id": "ENSP00000371003.1",
"transcript_support_level": 5,
"aa_start": 310,
"aa_end": null,
"aa_length": 602,
"cds_start": 929,
"cds_end": null,
"cds_length": 1809,
"cdna_start": 1182,
"cdna_end": null,
"cdna_length": 4229,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "ENST00000704301.1",
"protein_id": "ENSP00000515825.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 602,
"cds_start": 929,
"cds_end": null,
"cds_length": 1809,
"cdna_start": 1553,
"cdna_end": null,
"cdna_length": 4561,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.926T>G",
"hgvs_p": "p.Phe309Cys",
"transcript": "NM_001370115.2",
"protein_id": "NP_001357044.1",
"transcript_support_level": null,
"aa_start": 309,
"aa_end": null,
"aa_length": 601,
"cds_start": 926,
"cds_end": null,
"cds_length": 1806,
"cdna_start": 1038,
"cdna_end": null,
"cdna_length": 4082,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.926T>G",
"hgvs_p": "p.Phe309Cys",
"transcript": "ENST00000627286.2",
"protein_id": "ENSP00000487386.2",
"transcript_support_level": 5,
"aa_start": 309,
"aa_end": null,
"aa_length": 601,
"cds_start": 926,
"cds_end": null,
"cds_length": 1806,
"cdna_start": 997,
"cdna_end": null,
"cdna_length": 4020,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.878T>G",
"hgvs_p": "p.Phe293Cys",
"transcript": "NM_001330057.3",
"protein_id": "NP_001316986.1",
"transcript_support_level": null,
"aa_start": 293,
"aa_end": null,
"aa_length": 585,
"cds_start": 878,
"cds_end": null,
"cds_length": 1758,
"cdna_start": 1136,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 16,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.878T>G",
"hgvs_p": "p.Phe293Cys",
"transcript": "NM_001370112.2",
"protein_id": "NP_001357041.1",
"transcript_support_level": null,
"aa_start": 293,
"aa_end": null,
"aa_length": 585,
"cds_start": 878,
"cds_end": null,
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"cdna_start": 1148,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 9,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.863T>G",
"hgvs_p": "p.Phe288Cys",
"transcript": "NM_001370116.2",
"protein_id": "NP_001357045.1",
"transcript_support_level": null,
"aa_start": 288,
"aa_end": null,
"aa_length": 580,
"cds_start": 863,
"cds_end": null,
"cds_length": 1743,
"cdna_start": 906,
"cdna_end": null,
"cdna_length": 3950,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ZMYND11",
"gene_hgnc_id": 16966,
"hgvs_c": "c.929T>G",
"hgvs_p": "p.Phe310Cys",
"transcript": "NM_001370117.2",
"protein_id": "NP_001357046.1",
"transcript_support_level": null,
"aa_start": 310,
"aa_end": null,
"aa_length": 579,
"cds_start": 929,
"cds_end": null,
"cds_length": 1740,
"cdna_start": 1053,
"cdna_end": null,
"cdna_length": 4028,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "F",
"aa_alt": "C",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": null,
"intron_rank_end": null,
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}
],
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}