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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: 3-47504426-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=47504426&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 47504426,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "NM_001031703.3",
"consequences": [
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.227G>A",
"hgvs_p": "p.Arg76Gln",
"transcript": "NM_001031703.3",
"protein_id": "NP_001026873.2",
"transcript_support_level": null,
"aa_start": 76,
"aa_end": null,
"aa_length": 266,
"cds_start": 227,
"cds_end": null,
"cds_length": 801,
"cdna_start": 349,
"cdna_end": null,
"cdna_length": 1352,
"mane_select": "ENST00000296149.9",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.227G>A",
"hgvs_p": "p.Arg76Gln",
"transcript": "ENST00000296149.9",
"protein_id": "ENSP00000296149.4",
"transcript_support_level": 1,
"aa_start": 76,
"aa_end": null,
"aa_length": 266,
"cds_start": 227,
"cds_end": null,
"cds_length": 801,
"cdna_start": 349,
"cdna_end": null,
"cdna_length": 1352,
"mane_select": "NM_001031703.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.227G>A",
"hgvs_p": "p.Arg76Gln",
"transcript": "NM_001424210.1",
"protein_id": "NP_001411139.1",
"transcript_support_level": null,
"aa_start": 76,
"aa_end": null,
"aa_length": 274,
"cds_start": 227,
"cds_end": null,
"cds_length": 825,
"cdna_start": 349,
"cdna_end": null,
"cdna_length": 1376,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.218G>A",
"hgvs_p": "p.Arg73Gln",
"transcript": "NM_001424211.1",
"protein_id": "NP_001411140.1",
"transcript_support_level": null,
"aa_start": 73,
"aa_end": null,
"aa_length": 263,
"cds_start": 218,
"cds_end": null,
"cds_length": 792,
"cdna_start": 321,
"cdna_end": null,
"cdna_length": 1324,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.218G>A",
"hgvs_p": "p.Arg73Gln",
"transcript": "NM_001424212.1",
"protein_id": "NP_001411141.1",
"transcript_support_level": null,
"aa_start": 73,
"aa_end": null,
"aa_length": 263,
"cds_start": 218,
"cds_end": null,
"cds_length": 792,
"cdna_start": 583,
"cdna_end": null,
"cdna_length": 1586,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.218G>A",
"hgvs_p": "p.Arg73Gln",
"transcript": "NM_001424213.1",
"protein_id": "NP_001411142.1",
"transcript_support_level": null,
"aa_start": 73,
"aa_end": null,
"aa_length": 263,
"cds_start": 218,
"cds_end": null,
"cds_length": 792,
"cdna_start": 352,
"cdna_end": null,
"cdna_length": 1355,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.176G>A",
"hgvs_p": "p.Arg59Gln",
"transcript": "NM_001424214.1",
"protein_id": "NP_001411143.1",
"transcript_support_level": null,
"aa_start": 59,
"aa_end": null,
"aa_length": 249,
"cds_start": 176,
"cds_end": null,
"cds_length": 750,
"cdna_start": 328,
"cdna_end": null,
"cdna_length": 1331,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.227G>A",
"hgvs_p": "p.Arg76Gln",
"transcript": "NM_001424215.1",
"protein_id": "NP_001411144.1",
"transcript_support_level": null,
"aa_start": 76,
"aa_end": null,
"aa_length": 217,
"cds_start": 227,
"cds_end": null,
"cds_length": 654,
"cdna_start": 349,
"cdna_end": null,
"cdna_length": 1205,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.80G>A",
"hgvs_p": "p.Arg27Gln",
"transcript": "NM_001424216.1",
"protein_id": "NP_001411145.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 217,
"cds_start": 80,
"cds_end": null,
"cds_length": 654,
"cdna_start": 278,
"cdna_end": null,
"cdna_length": 1281,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.80G>A",
"hgvs_p": "p.Arg27Gln",
"transcript": "NM_001424217.1",
"protein_id": "NP_001411146.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 217,
"cds_start": 80,
"cds_end": null,
"cds_length": 654,
"cdna_start": 456,
"cdna_end": null,
"cdna_length": 1459,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.80G>A",
"hgvs_p": "p.Arg27Gln",
"transcript": "NM_001424218.1",
"protein_id": "NP_001411147.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
"aa_length": 217,
"cds_start": 80,
"cds_end": null,
"cds_length": 654,
"cdna_start": 194,
"cdna_end": null,
"cdna_length": 1197,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 2,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.77G>A",
"hgvs_p": "p.Arg26Gln",
"transcript": "NM_001424219.1",
"protein_id": "NP_001411148.1",
"transcript_support_level": null,
"aa_start": 26,
"aa_end": null,
"aa_length": 216,
"cds_start": 77,
"cds_end": null,
"cds_length": 651,
"cdna_start": 199,
"cdna_end": null,
"cdna_length": 1202,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.8G>A",
"hgvs_p": "p.Arg3Gln",
"transcript": "NM_001363957.1",
"protein_id": "NP_001350886.1",
"transcript_support_level": null,
"aa_start": 3,
"aa_end": null,
"aa_length": 193,
"cds_start": 8,
"cds_end": null,
"cds_length": 582,
"cdna_start": 527,
"cdna_end": null,
"cdna_length": 1530,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.8G>A",
"hgvs_p": "p.Arg3Gln",
"transcript": "NM_001424220.1",
"protein_id": "NP_001411149.1",
"transcript_support_level": null,
"aa_start": 3,
"aa_end": null,
"aa_length": 193,
"cds_start": 8,
"cds_end": null,
"cds_length": 582,
"cdna_start": 265,
"cdna_end": null,
"cdna_length": 1268,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.8G>A",
"hgvs_p": "p.Arg3Gln",
"transcript": "NM_001424222.1",
"protein_id": "NP_001411151.1",
"transcript_support_level": null,
"aa_start": 3,
"aa_end": null,
"aa_length": 193,
"cds_start": 8,
"cds_end": null,
"cds_length": 582,
"cdna_start": 456,
"cdna_end": null,
"cdna_length": 1459,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.8G>A",
"hgvs_p": "p.Arg3Gln",
"transcript": "NM_001424223.1",
"protein_id": "NP_001411152.1",
"transcript_support_level": null,
"aa_start": 3,
"aa_end": null,
"aa_length": 193,
"cds_start": 8,
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"cdna_start": 735,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.8G>A",
"hgvs_p": "p.Arg3Gln",
"transcript": "NM_001424224.1",
"protein_id": "NP_001411153.1",
"transcript_support_level": null,
"aa_start": 3,
"aa_end": null,
"aa_length": 193,
"cds_start": 8,
"cds_end": null,
"cds_length": 582,
"cdna_start": 296,
"cdna_end": null,
"cdna_length": 1299,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.8G>A",
"hgvs_p": "p.Arg3Gln",
"transcript": "NM_001424225.1",
"protein_id": "NP_001411154.1",
"transcript_support_level": null,
"aa_start": 3,
"aa_end": null,
"aa_length": 193,
"cds_start": 8,
"cds_end": null,
"cds_length": 582,
"cdna_start": 384,
"cdna_end": null,
"cdna_length": 1387,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.8G>A",
"hgvs_p": "p.Arg3Gln",
"transcript": "NM_001424226.1",
"protein_id": "NP_001411155.1",
"transcript_support_level": null,
"aa_start": 3,
"aa_end": null,
"aa_length": 193,
"cds_start": 8,
"cds_end": null,
"cds_length": 582,
"cdna_start": 372,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.8G>A",
"hgvs_p": "p.Arg3Gln",
"transcript": "NM_001424227.1",
"protein_id": "NP_001411156.1",
"transcript_support_level": null,
"aa_start": 3,
"aa_end": null,
"aa_length": 193,
"cds_start": 8,
"cds_end": null,
"cds_length": 582,
"cdna_start": 883,
"cdna_end": null,
"cdna_length": 1886,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 4,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.8G>A",
"hgvs_p": "p.Arg3Gln",
"transcript": "ENST00000439305.5",
"protein_id": "ENSP00000402399.1",
"transcript_support_level": 2,
"aa_start": 3,
"aa_end": null,
"aa_length": 193,
"cds_start": 8,
"cds_end": null,
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"cdna_start": 266,
"cdna_end": null,
"cdna_length": 880,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.8G>A",
"hgvs_p": "p.Arg3Gln",
"transcript": "ENST00000446787.5",
"protein_id": "ENSP00000412593.1",
"transcript_support_level": 3,
"aa_start": 3,
"aa_end": null,
"aa_length": 193,
"cds_start": 8,
"cds_end": null,
"cds_length": 582,
"cdna_start": 197,
"cdna_end": null,
"cdna_length": 894,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "R",
"aa_alt": "Q",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 3,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "ELP6",
"gene_hgnc_id": 25976,
"hgvs_c": "c.80G>A",
"hgvs_p": "p.Arg27Gln",
"transcript": "NM_001424228.1",
"protein_id": "NP_001411157.1",
"transcript_support_level": null,
"aa_start": 27,
"aa_end": null,
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}