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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: 14-73254537-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=14&pos=73254537&ref=G&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "14",
"pos": 73254537,
"ref": "G",
"alt": "A",
"effect": "missense_variant",
"transcript": "NM_001365906.3",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "NM_001365906.3",
"protein_id": "NP_001352835.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1278,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3837,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000644200.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001365906.3"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "ENST00000644200.2",
"protein_id": "ENSP00000495882.2",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1278,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3837,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_001365906.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000644200.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "n.1327G>A",
"hgvs_p": null,
"transcript": "ENST00000216658.9",
"protein_id": "ENSP00000216658.5",
"transcript_support_level": 1,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000216658.9"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"non_coding_transcript_exon_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "n.1246G>A",
"hgvs_p": null,
"transcript": "ENST00000555123.5",
"protein_id": "ENSP00000452455.1",
"transcript_support_level": 1,
"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": null,
"mane_select": null,
"mane_plus": null,
"biotype": "nonsense_mediated_decay",
"feature": "ENST00000555123.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1420G>A",
"hgvs_p": "p.Val474Ile",
"transcript": "ENST00000957731.1",
"protein_id": "ENSP00000627790.1",
"transcript_support_level": null,
"aa_start": 474,
"aa_end": null,
"aa_length": 1309,
"cds_start": 1420,
"cds_end": null,
"cds_length": 3930,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957731.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1393G>A",
"hgvs_p": "p.Val465Ile",
"transcript": "ENST00000911608.1",
"protein_id": "ENSP00000581667.1",
"transcript_support_level": null,
"aa_start": 465,
"aa_end": null,
"aa_length": 1300,
"cds_start": 1393,
"cds_end": null,
"cds_length": 3903,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000911608.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "ENST00000554301.5",
"protein_id": "ENSP00000451803.1",
"transcript_support_level": 2,
"aa_start": 443,
"aa_end": null,
"aa_length": 1278,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3837,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000554301.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "ENST00000911607.1",
"protein_id": "ENSP00000581666.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1278,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3837,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000911607.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "ENST00000957729.1",
"protein_id": "ENSP00000627788.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1278,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3837,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957729.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "ENST00000957732.1",
"protein_id": "ENSP00000627791.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1278,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3837,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957732.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "NM_001365907.2",
"protein_id": "NP_001352836.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1262,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001365907.2"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "ENST00000555445.5",
"protein_id": "ENSP00000451729.1",
"transcript_support_level": 2,
"aa_start": 443,
"aa_end": null,
"aa_length": 1262,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3789,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000555445.5"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1246G>A",
"hgvs_p": "p.Val416Ile",
"transcript": "NM_173462.4",
"protein_id": "NP_775733.3",
"transcript_support_level": null,
"aa_start": 416,
"aa_end": null,
"aa_length": 1251,
"cds_start": 1246,
"cds_end": null,
"cds_length": 3756,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_173462.4"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1246G>A",
"hgvs_p": "p.Val416Ile",
"transcript": "ENST00000340738.9",
"protein_id": "ENSP00000345395.5",
"transcript_support_level": 5,
"aa_start": 416,
"aa_end": null,
"aa_length": 1251,
"cds_start": 1246,
"cds_end": null,
"cds_length": 3756,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000340738.9"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "ENST00000864046.1",
"protein_id": "ENSP00000534105.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1199,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3600,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000864046.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "ENST00000911606.1",
"protein_id": "ENSP00000581665.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1199,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3600,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000911606.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "ENST00000957733.1",
"protein_id": "ENSP00000627792.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1199,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3600,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957733.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 24,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "ENST00000957730.1",
"protein_id": "ENSP00000627789.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1079,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3240,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000957730.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1408G>A",
"hgvs_p": "p.Val470Ile",
"transcript": "XM_047431872.1",
"protein_id": "XP_047287828.1",
"transcript_support_level": null,
"aa_start": 470,
"aa_end": null,
"aa_length": 1305,
"cds_start": 1408,
"cds_end": null,
"cds_length": 3918,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047431872.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 12,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1348G>A",
"hgvs_p": "p.Val450Ile",
"transcript": "XM_047431875.1",
"protein_id": "XP_047287831.1",
"transcript_support_level": null,
"aa_start": 450,
"aa_end": null,
"aa_length": 1285,
"cds_start": 1348,
"cds_end": null,
"cds_length": 3858,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047431875.1"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 14,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "XM_011537291.4",
"protein_id": "XP_011535593.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1278,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3837,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_011537291.4"
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "PAPLN",
"gene_hgnc_id": 19262,
"hgvs_c": "c.1327G>A",
"hgvs_p": "p.Val443Ile",
"transcript": "XM_011537292.4",
"protein_id": "XP_011535594.1",
"transcript_support_level": null,
"aa_start": 443,
"aa_end": null,
"aa_length": 1278,
"cds_start": 1327,
"cds_end": null,
"cds_length": 3837,
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}