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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: 5-41201565-T-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=41201565&ref=T&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 41201565,
"ref": "T",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_000065.5",
"consequences": [
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "NM_000065.5",
"protein_id": "NP_000056.2",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 934,
"cds_start": 293,
"cds_end": null,
"cds_length": 2805,
"cdna_start": 470,
"cdna_end": null,
"cdna_length": 3691,
"mane_select": "ENST00000337836.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_000065.5"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000337836.10",
"protein_id": "ENSP00000338861.5",
"transcript_support_level": 1,
"aa_start": 98,
"aa_end": null,
"aa_length": 934,
"cds_start": 293,
"cds_end": null,
"cds_length": 2805,
"cdna_start": 470,
"cdna_end": null,
"cdna_length": 3691,
"mane_select": "NM_000065.5",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000337836.10"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000263413.7",
"protein_id": "ENSP00000263413.3",
"transcript_support_level": 1,
"aa_start": 98,
"aa_end": null,
"aa_length": 934,
"cds_start": 293,
"cds_end": null,
"cds_length": 2805,
"cdna_start": 558,
"cdna_end": null,
"cdna_length": 3661,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000263413.7"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905250.1",
"protein_id": "ENSP00000575309.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 962,
"cds_start": 293,
"cds_end": null,
"cds_length": 2889,
"cdna_start": 470,
"cdna_end": null,
"cdna_length": 3773,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905250.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905256.1",
"protein_id": "ENSP00000575315.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 953,
"cds_start": 293,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 485,
"cdna_end": null,
"cdna_length": 3613,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905256.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905270.1",
"protein_id": "ENSP00000575329.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 953,
"cds_start": 293,
"cds_end": null,
"cds_length": 2862,
"cdna_start": 567,
"cdna_end": null,
"cdna_length": 3520,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905270.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905249.1",
"protein_id": "ENSP00000575308.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 943,
"cds_start": 293,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 480,
"cdna_end": null,
"cdna_length": 5608,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905249.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905265.1",
"protein_id": "ENSP00000575324.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 943,
"cds_start": 293,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 609,
"cdna_end": null,
"cdna_length": 3532,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905265.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905279.1",
"protein_id": "ENSP00000575338.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 943,
"cds_start": 293,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 480,
"cdna_end": null,
"cdna_length": 3411,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905279.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905280.1",
"protein_id": "ENSP00000575339.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 943,
"cds_start": 293,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 596,
"cdna_end": null,
"cdna_length": 3527,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905280.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905281.1",
"protein_id": "ENSP00000575340.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 943,
"cds_start": 293,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 591,
"cdna_end": null,
"cdna_length": 3522,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905281.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000942840.1",
"protein_id": "ENSP00000612899.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 943,
"cds_start": 293,
"cds_end": null,
"cds_length": 2832,
"cdna_start": 570,
"cdna_end": null,
"cdna_length": 3491,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942840.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000942839.1",
"protein_id": "ENSP00000612898.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 936,
"cds_start": 293,
"cds_end": null,
"cds_length": 2811,
"cdna_start": 462,
"cdna_end": null,
"cdna_length": 3376,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000942839.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 18,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "NM_001115131.4",
"protein_id": "NP_001108603.2",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 934,
"cds_start": 293,
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"cdna_start": 589,
"cdna_end": null,
"cdna_length": 3810,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001115131.4"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905252.1",
"protein_id": "ENSP00000575311.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 934,
"cds_start": 293,
"cds_end": null,
"cds_length": 2805,
"cdna_start": 652,
"cdna_end": null,
"cdna_length": 3752,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905252.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905254.1",
"protein_id": "ENSP00000575313.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 934,
"cds_start": 293,
"cds_end": null,
"cds_length": 2805,
"cdna_start": 618,
"cdna_end": null,
"cdna_length": 3718,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905254.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905257.1",
"protein_id": "ENSP00000575316.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 934,
"cds_start": 293,
"cds_end": null,
"cds_length": 2805,
"cdna_start": 619,
"cdna_end": null,
"cdna_length": 3690,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905257.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905259.1",
"protein_id": "ENSP00000575318.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 934,
"cds_start": 293,
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"cdna_start": 627,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905259.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905261.1",
"protein_id": "ENSP00000575320.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 934,
"cds_start": 293,
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"cds_length": 2805,
"cdna_start": 647,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905261.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905267.1",
"protein_id": "ENSP00000575326.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
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"cds_start": 293,
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"cdna_start": 544,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905267.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905269.1",
"protein_id": "ENSP00000575328.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 934,
"cds_start": 293,
"cds_end": null,
"cds_length": 2805,
"cdna_start": 620,
"cdna_end": null,
"cdna_length": 3516,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905269.1"
},
{
"aa_ref": "E",
"aa_alt": "G",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 19,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "C6",
"gene_hgnc_id": 1339,
"hgvs_c": "c.293A>G",
"hgvs_p": "p.Glu98Gly",
"transcript": "ENST00000905271.1",
"protein_id": "ENSP00000575330.1",
"transcript_support_level": null,
"aa_start": 98,
"aa_end": null,
"aa_length": 934,
"cds_start": 293,
"cds_end": null,
"cds_length": 2805,
"cdna_start": 616,
"cdna_end": null,
"cdna_length": 3834,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000905271.1"
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}