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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: 12-6578867-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=6578867&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 6578867,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_001273.5",
"consequences": [
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4960C>G",
"hgvs_p": "p.Pro1654Ala",
"transcript": "NM_001273.5",
"protein_id": "NP_001264.2",
"transcript_support_level": null,
"aa_start": 1654,
"aa_end": null,
"aa_length": 1912,
"cds_start": 4960,
"cds_end": null,
"cds_length": 5739,
"cdna_start": 5118,
"cdna_end": null,
"cdna_length": 6491,
"mane_select": "ENST00000544040.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001273.5"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4960C>G",
"hgvs_p": "p.Pro1654Ala",
"transcript": "ENST00000544040.7",
"protein_id": "ENSP00000440542.2",
"transcript_support_level": 5,
"aa_start": 1654,
"aa_end": null,
"aa_length": 1912,
"cds_start": 4960,
"cds_end": null,
"cds_length": 5739,
"cdna_start": 5118,
"cdna_end": null,
"cdna_length": 6491,
"mane_select": "NM_001273.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000544040.7"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4927C>G",
"hgvs_p": "p.Pro1643Ala",
"transcript": "ENST00000357008.7",
"protein_id": "ENSP00000349508.3",
"transcript_support_level": 1,
"aa_start": 1643,
"aa_end": null,
"aa_length": 1902,
"cds_start": 4927,
"cds_end": null,
"cds_length": 5709,
"cdna_start": 5062,
"cdna_end": null,
"cdna_length": 6438,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000357008.7"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": false,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000285238",
"gene_hgnc_id": null,
"hgvs_c": "n.*41C>G",
"hgvs_p": null,
"transcript": "ENST00000644480.2",
"protein_id": "ENSP00000493629.2",
"transcript_support_level": null,
"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": 8502,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000644480.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": false,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ENSG00000285238",
"gene_hgnc_id": null,
"hgvs_c": "n.*41C>G",
"hgvs_p": null,
"transcript": "ENST00000644480.2",
"protein_id": "ENSP00000493629.2",
"transcript_support_level": null,
"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": 8502,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000644480.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "ENSG00000285238",
"gene_hgnc_id": null,
"hgvs_c": "n.9+8517C>G",
"hgvs_p": null,
"transcript": "ENST00000646322.1",
"protein_id": "ENSP00000494949.1",
"transcript_support_level": null,
"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": 2356,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000646322.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.5044C>G",
"hgvs_p": "p.Pro1682Ala",
"transcript": "ENST00000645095.1",
"protein_id": "ENSP00000496634.1",
"transcript_support_level": null,
"aa_start": 1682,
"aa_end": null,
"aa_length": 1940,
"cds_start": 5044,
"cds_end": null,
"cds_length": 5823,
"cdna_start": 5044,
"cdna_end": null,
"cdna_length": 6291,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000645095.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 33,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.5035C>G",
"hgvs_p": "p.Pro1679Ala",
"transcript": "ENST00000544484.6",
"protein_id": "ENSP00000440392.1",
"transcript_support_level": 2,
"aa_start": 1679,
"aa_end": null,
"aa_length": 1937,
"cds_start": 5035,
"cds_end": null,
"cds_length": 5814,
"cdna_start": 5182,
"cdna_end": null,
"cdna_length": 6555,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000544484.6"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 32,
"exon_rank_end": null,
"exon_count": 38,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4984C>G",
"hgvs_p": "p.Pro1662Ala",
"transcript": "ENST00000642879.1",
"protein_id": "ENSP00000494456.1",
"transcript_support_level": null,
"aa_start": 1662,
"aa_end": null,
"aa_length": 1920,
"cds_start": 4984,
"cds_end": null,
"cds_length": 5763,
"cdna_start": 5045,
"cdna_end": null,
"cdna_length": 6309,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000642879.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4966C>G",
"hgvs_p": "p.Pro1656Ala",
"transcript": "ENST00000931052.1",
"protein_id": "ENSP00000601111.1",
"transcript_support_level": null,
"aa_start": 1656,
"aa_end": null,
"aa_length": 1915,
"cds_start": 4966,
"cds_end": null,
"cds_length": 5748,
"cdna_start": 5125,
"cdna_end": null,
"cdna_length": 6449,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931052.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4966C>G",
"hgvs_p": "p.Pro1656Ala",
"transcript": "ENST00000645005.1",
"protein_id": "ENSP00000493471.1",
"transcript_support_level": null,
"aa_start": 1656,
"aa_end": null,
"aa_length": 1914,
"cds_start": 4966,
"cds_end": null,
"cds_length": 5745,
"cdna_start": 5142,
"cdna_end": null,
"cdna_length": 6175,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000645005.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4960C>G",
"hgvs_p": "p.Pro1654Ala",
"transcript": "ENST00000931051.1",
"protein_id": "ENSP00000601110.1",
"transcript_support_level": null,
"aa_start": 1654,
"aa_end": null,
"aa_length": 1913,
"cds_start": 4960,
"cds_end": null,
"cds_length": 5742,
"cdna_start": 5116,
"cdna_end": null,
"cdna_length": 6487,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931051.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4945C>G",
"hgvs_p": "p.Pro1649Ala",
"transcript": "ENST00000931042.1",
"protein_id": "ENSP00000601101.1",
"transcript_support_level": null,
"aa_start": 1649,
"aa_end": null,
"aa_length": 1908,
"cds_start": 4945,
"cds_end": null,
"cds_length": 5727,
"cdna_start": 5251,
"cdna_end": null,
"cdna_length": 6627,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931042.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4945C>G",
"hgvs_p": "p.Pro1649Ala",
"transcript": "ENST00000931045.1",
"protein_id": "ENSP00000601104.1",
"transcript_support_level": null,
"aa_start": 1649,
"aa_end": null,
"aa_length": 1907,
"cds_start": 4945,
"cds_end": null,
"cds_length": 5724,
"cdna_start": 5203,
"cdna_end": null,
"cdna_length": 6576,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931045.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 33,
"exon_rank_end": null,
"exon_count": 39,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4939C>G",
"hgvs_p": "p.Pro1647Ala",
"transcript": "NM_001297553.2",
"protein_id": "NP_001284482.1",
"transcript_support_level": null,
"aa_start": 1647,
"aa_end": null,
"aa_length": 1905,
"cds_start": 4939,
"cds_end": null,
"cds_length": 5718,
"cdna_start": 5017,
"cdna_end": null,
"cdna_length": 6390,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001297553.2"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4939C>G",
"hgvs_p": "p.Pro1647Ala",
"transcript": "ENST00000645022.1",
"protein_id": "ENSP00000496163.1",
"transcript_support_level": null,
"aa_start": 1647,
"aa_end": null,
"aa_length": 1905,
"cds_start": 4939,
"cds_end": null,
"cds_length": 5718,
"cdna_start": 5300,
"cdna_end": null,
"cdna_length": 6673,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000645022.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4939C>G",
"hgvs_p": "p.Pro1647Ala",
"transcript": "ENST00000957180.1",
"protein_id": "ENSP00000627239.1",
"transcript_support_level": null,
"aa_start": 1647,
"aa_end": null,
"aa_length": 1905,
"cds_start": 4939,
"cds_end": null,
"cds_length": 5718,
"cdna_start": 5243,
"cdna_end": null,
"cdna_length": 6615,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957180.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4936C>G",
"hgvs_p": "p.Pro1646Ala",
"transcript": "ENST00000931049.1",
"protein_id": "ENSP00000601108.1",
"transcript_support_level": null,
"aa_start": 1646,
"aa_end": null,
"aa_length": 1904,
"cds_start": 4936,
"cds_end": null,
"cds_length": 5715,
"cdna_start": 5107,
"cdna_end": null,
"cdna_length": 6480,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000931049.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4936C>G",
"hgvs_p": "p.Pro1646Ala",
"transcript": "ENST00000957179.1",
"protein_id": "ENSP00000627238.1",
"transcript_support_level": null,
"aa_start": 1646,
"aa_end": null,
"aa_length": 1904,
"cds_start": 4936,
"cds_end": null,
"cds_length": 5715,
"cdna_start": 5163,
"cdna_end": null,
"cdna_length": 6460,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957179.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 35,
"exon_rank_end": null,
"exon_count": 41,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4933C>G",
"hgvs_p": "p.Pro1645Ala",
"transcript": "ENST00000643335.1",
"protein_id": "ENSP00000496358.1",
"transcript_support_level": null,
"aa_start": 1645,
"aa_end": null,
"aa_length": 1903,
"cds_start": 4933,
"cds_end": null,
"cds_length": 5712,
"cdna_start": 5140,
"cdna_end": null,
"cdna_length": 6411,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000643335.1"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4927C>G",
"hgvs_p": "p.Pro1643Ala",
"transcript": "NM_001363606.2",
"protein_id": "NP_001350535.1",
"transcript_support_level": null,
"aa_start": 1643,
"aa_end": null,
"aa_length": 1902,
"cds_start": 4927,
"cds_end": null,
"cds_length": 5709,
"cdna_start": 5085,
"cdna_end": null,
"cdna_length": 6461,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001363606.2"
},
{
"aa_ref": "P",
"aa_alt": "A",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 34,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CHD4",
"gene_hgnc_id": 1919,
"hgvs_c": "c.4927C>G",
"hgvs_p": "p.Pro1643Ala",
"transcript": "ENST00000931048.1",
"protein_id": "ENSP00000601107.1",
"transcript_support_level": null,
"aa_start": 1643,
"aa_end": null,
"aa_length": 1901,
"cds_start": 4927,
"cds_end": null,
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}
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}