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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: X-45110125-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=X&pos=45110125&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "X",
"pos": 45110125,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001419809.1",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4208G>A",
"hgvs_p": "p.Arg1403Gln",
"transcript": "NM_001291415.2",
"protein_id": "NP_001278344.1",
"transcript_support_level": null,
"aa_start": 1403,
"aa_end": null,
"aa_length": 1453,
"cds_start": 4208,
"cds_end": null,
"cds_length": 4362,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000611820.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001291415.2"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4208G>A",
"hgvs_p": "p.Arg1403Gln",
"transcript": "ENST00000611820.5",
"protein_id": "ENSP00000483595.2",
"transcript_support_level": 1,
"aa_start": 1403,
"aa_end": null,
"aa_length": 1453,
"cds_start": 4208,
"cds_end": null,
"cds_length": 4362,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001291415.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000611820.5"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4073G>A",
"hgvs_p": "p.Arg1358Gln",
"transcript": "ENST00000382899.9",
"protein_id": "ENSP00000372355.6",
"transcript_support_level": 1,
"aa_start": 1358,
"aa_end": null,
"aa_length": 1408,
"cds_start": 4073,
"cds_end": null,
"cds_length": 4227,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000382899.9"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4052G>A",
"hgvs_p": "p.Arg1351Gln",
"transcript": "ENST00000377967.9",
"protein_id": "ENSP00000367203.4",
"transcript_support_level": 1,
"aa_start": 1351,
"aa_end": null,
"aa_length": 1401,
"cds_start": 4052,
"cds_end": null,
"cds_length": 4206,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000377967.9"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.3917G>A",
"hgvs_p": "p.Arg1306Gln",
"transcript": "ENST00000536777.6",
"protein_id": "ENSP00000437405.3",
"transcript_support_level": 1,
"aa_start": 1306,
"aa_end": null,
"aa_length": 1356,
"cds_start": 3917,
"cds_end": null,
"cds_length": 4071,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000536777.6"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.3815G>A",
"hgvs_p": "p.Arg1272Gln",
"transcript": "ENST00000543216.6",
"protein_id": "ENSP00000443078.3",
"transcript_support_level": 1,
"aa_start": 1272,
"aa_end": null,
"aa_length": 1322,
"cds_start": 3815,
"cds_end": null,
"cds_length": 3969,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000543216.6"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 30,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4316G>A",
"hgvs_p": "p.Arg1439Gln",
"transcript": "NM_001419809.1",
"protein_id": "NP_001406738.1",
"transcript_support_level": null,
"aa_start": 1439,
"aa_end": null,
"aa_length": 1489,
"cds_start": 4316,
"cds_end": null,
"cds_length": 4470,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001419809.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4214G>A",
"hgvs_p": "p.Arg1405Gln",
"transcript": "NM_001419810.1",
"protein_id": "NP_001406739.1",
"transcript_support_level": null,
"aa_start": 1405,
"aa_end": null,
"aa_length": 1455,
"cds_start": 4214,
"cds_end": null,
"cds_length": 4368,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001419810.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4181G>A",
"hgvs_p": "p.Arg1394Gln",
"transcript": "NM_001419811.1",
"protein_id": "NP_001406740.1",
"transcript_support_level": null,
"aa_start": 1394,
"aa_end": null,
"aa_length": 1444,
"cds_start": 4181,
"cds_end": null,
"cds_length": 4335,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001419811.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4160G>A",
"hgvs_p": "p.Arg1387Gln",
"transcript": "NM_001419812.1",
"protein_id": "NP_001406741.1",
"transcript_support_level": null,
"aa_start": 1387,
"aa_end": null,
"aa_length": 1437,
"cds_start": 4160,
"cds_end": null,
"cds_length": 4314,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001419812.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 29,
"exon_rank_end": null,
"exon_count": 30,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4130G>A",
"hgvs_p": "p.Arg1377Gln",
"transcript": "ENST00000674586.1",
"protein_id": "ENSP00000502660.1",
"transcript_support_level": null,
"aa_start": 1377,
"aa_end": null,
"aa_length": 1427,
"cds_start": 4130,
"cds_end": null,
"cds_length": 4284,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000674586.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4106G>A",
"hgvs_p": "p.Arg1369Gln",
"transcript": "NM_001419813.1",
"protein_id": "NP_001406742.1",
"transcript_support_level": null,
"aa_start": 1369,
"aa_end": null,
"aa_length": 1419,
"cds_start": 4106,
"cds_end": null,
"cds_length": 4260,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001419813.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4106G>A",
"hgvs_p": "p.Arg1369Gln",
"transcript": "ENST00000867282.1",
"protein_id": "ENSP00000537341.1",
"transcript_support_level": null,
"aa_start": 1369,
"aa_end": null,
"aa_length": 1419,
"cds_start": 4106,
"cds_end": null,
"cds_length": 4260,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000867282.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4073G>A",
"hgvs_p": "p.Arg1358Gln",
"transcript": "NM_001291416.2",
"protein_id": "NP_001278345.1",
"transcript_support_level": null,
"aa_start": 1358,
"aa_end": null,
"aa_length": 1408,
"cds_start": 4073,
"cds_end": null,
"cds_length": 4227,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001291416.2"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4058G>A",
"hgvs_p": "p.Arg1353Gln",
"transcript": "NM_001419814.1",
"protein_id": "NP_001406743.1",
"transcript_support_level": null,
"aa_start": 1353,
"aa_end": null,
"aa_length": 1403,
"cds_start": 4058,
"cds_end": null,
"cds_length": 4212,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001419814.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4052G>A",
"hgvs_p": "p.Arg1351Gln",
"transcript": "NM_021140.4",
"protein_id": "NP_066963.2",
"transcript_support_level": null,
"aa_start": 1351,
"aa_end": null,
"aa_length": 1401,
"cds_start": 4052,
"cds_end": null,
"cds_length": 4206,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_021140.4"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 28,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.4046G>A",
"hgvs_p": "p.Arg1349Gln",
"transcript": "ENST00000867283.1",
"protein_id": "ENSP00000537342.1",
"transcript_support_level": null,
"aa_start": 1349,
"aa_end": null,
"aa_length": 1399,
"cds_start": 4046,
"cds_end": null,
"cds_length": 4200,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000867283.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.3971G>A",
"hgvs_p": "p.Arg1324Gln",
"transcript": "ENST00000683021.1",
"protein_id": "ENSP00000507416.1",
"transcript_support_level": null,
"aa_start": 1324,
"aa_end": null,
"aa_length": 1374,
"cds_start": 3971,
"cds_end": null,
"cds_length": 4125,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000683021.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.3950G>A",
"hgvs_p": "p.Arg1317Gln",
"transcript": "NM_001410742.1",
"protein_id": "NP_001397671.1",
"transcript_support_level": null,
"aa_start": 1317,
"aa_end": null,
"aa_length": 1367,
"cds_start": 3950,
"cds_end": null,
"cds_length": 4104,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001410742.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.3950G>A",
"hgvs_p": "p.Arg1317Gln",
"transcript": "ENST00000675577.1",
"protein_id": "ENSP00000501855.1",
"transcript_support_level": null,
"aa_start": 1317,
"aa_end": null,
"aa_length": 1367,
"cds_start": 3950,
"cds_end": null,
"cds_length": 4104,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000675577.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.3923G>A",
"hgvs_p": "p.Arg1308Gln",
"transcript": "NM_001419815.1",
"protein_id": "NP_001406744.1",
"transcript_support_level": null,
"aa_start": 1308,
"aa_end": null,
"aa_length": 1358,
"cds_start": 3923,
"cds_end": null,
"cds_length": 4077,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001419815.1"
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 27,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "KDM6A",
"gene_hgnc_id": 12637,
"hgvs_c": "c.3917G>A",
"hgvs_p": "p.Arg1306Gln",
"transcript": "NM_001291417.2",
"protein_id": "NP_001278346.1",
"transcript_support_level": null,
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}