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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: 2-61492337-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=61492337&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 61492337,
"ref": "C",
"alt": "G",
"effect": "missense_variant",
"transcript": "ENST00000401558.7",
"consequences": [
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "NM_003400.4",
"protein_id": "NP_003391.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 2512,
"cdna_end": null,
"cdna_length": 4988,
"mane_select": "ENST00000401558.7",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000401558.7",
"protein_id": "ENSP00000384863.2",
"transcript_support_level": 1,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 2512,
"cdna_end": null,
"cdna_length": 4988,
"mane_select": "NM_003400.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000406957.5",
"protein_id": "ENSP00000385559.1",
"transcript_support_level": 1,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 1854,
"cdna_end": null,
"cdna_length": 3479,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000404992.6",
"protein_id": "ENSP00000385942.2",
"transcript_support_level": 2,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 2118,
"cdna_end": null,
"cdna_length": 4105,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000676553.1",
"protein_id": "ENSP00000504247.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 1967,
"cdna_end": null,
"cdna_length": 4603,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000676667.1",
"protein_id": "ENSP00000503809.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 3165,
"cdna_end": null,
"cdna_length": 5801,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000677150.1",
"protein_id": "ENSP00000503167.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 2005,
"cdna_end": null,
"cdna_length": 4641,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000677239.1",
"protein_id": "ENSP00000504087.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 2140,
"cdna_end": null,
"cdna_length": 4776,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000677417.1",
"protein_id": "ENSP00000503572.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 1816,
"cdna_end": null,
"cdna_length": 4452,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000677813.1",
"protein_id": "ENSP00000504543.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 1913,
"cdna_end": null,
"cdna_length": 4549,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000677814.1",
"protein_id": "ENSP00000504848.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 1864,
"cdna_end": null,
"cdna_length": 4500,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 17,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000677928.1",
"protein_id": "ENSP00000504198.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 1958,
"cdna_end": null,
"cdna_length": 4594,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000677933.1",
"protein_id": "ENSP00000503482.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 2060,
"cdna_end": null,
"cdna_length": 4696,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000678182.1",
"protein_id": "ENSP00000504594.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
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"cdna_start": 2057,
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"cdna_length": 4693,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000678790.1",
"protein_id": "ENSP00000503419.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1071,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3216,
"cdna_start": 1974,
"cdna_end": null,
"cdna_length": 4610,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1666G>C",
"hgvs_p": "p.Glu556Gln",
"transcript": "ENST00000676771.1",
"protein_id": "ENSP00000503808.1",
"transcript_support_level": null,
"aa_start": 556,
"aa_end": null,
"aa_length": 1056,
"cds_start": 1666,
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"cds_length": 3171,
"cdna_start": 1804,
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"cdna_length": 4440,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "NM_001410799.1",
"protein_id": "NP_001397728.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1026,
"cds_start": 1711,
"cds_end": null,
"cds_length": 3081,
"cdna_start": 2095,
"cdna_end": null,
"cdna_length": 4436,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000676999.1",
"protein_id": "ENSP00000502940.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
"aa_length": 1026,
"cds_start": 1711,
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"cds_length": 3081,
"cdna_start": 1798,
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"cdna_length": 4299,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000678081.1",
"protein_id": "ENSP00000503194.1",
"transcript_support_level": null,
"aa_start": 571,
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"cdna_start": 1936,
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"mane_select": null,
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"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 15,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1711G>C",
"hgvs_p": "p.Glu571Gln",
"transcript": "ENST00000676789.1",
"protein_id": "ENSP00000504617.1",
"transcript_support_level": null,
"aa_start": 571,
"aa_end": null,
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"cds_start": 1711,
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"cdna_start": 1936,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1495G>C",
"hgvs_p": "p.Glu499Gln",
"transcript": "ENST00000677803.1",
"protein_id": "ENSP00000503702.1",
"transcript_support_level": null,
"aa_start": 499,
"aa_end": null,
"aa_length": 999,
"cds_start": 1495,
"cds_end": null,
"cds_length": 3000,
"cdna_start": 1734,
"cdna_end": null,
"cdna_length": 4370,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "XPO1",
"gene_hgnc_id": 12825,
"hgvs_c": "c.1435G>C",
"hgvs_p": "p.Glu479Gln",
"transcript": "ENST00000678877.1",
"protein_id": "ENSP00000502889.1",
"transcript_support_level": null,
"aa_start": 479,
"aa_end": null,
"aa_length": 979,
"cds_start": 1435,
"cds_end": null,
"cds_length": 2940,
"cdna_start": 1603,
"cdna_end": null,
"cdna_length": 4239,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "E",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 23,
"intron_rank": null,
"intron_rank_end": null,
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{
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],
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"clinvar_review_status": "",
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"custom_annotations": null
}
],
"message": null
}