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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: 3-52694933-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=52694933&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 52694933,
"ref": "G",
"alt": "C",
"effect": "missense_variant",
"transcript": "NM_018446.4",
"consequences": [
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "NM_018446.4",
"protein_id": "NP_060916.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1409,
"cdna_end": null,
"cdna_length": 1856,
"mane_select": "ENST00000266014.11",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_018446.4"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000266014.11",
"protein_id": "ENSP00000266014.5",
"transcript_support_level": 1,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1409,
"cdna_end": null,
"cdna_length": 1856,
"mane_select": "NM_018446.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000266014.11"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000394783.7",
"protein_id": "ENSP00000378263.3",
"transcript_support_level": 1,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1180,
"cdna_end": null,
"cdna_length": 1621,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000394783.7"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000478968.6",
"protein_id": "ENSP00000419612.2",
"transcript_support_level": 1,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1382,
"cdna_end": null,
"cdna_length": 1826,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000478968.6"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "NM_001010983.3",
"protein_id": "NP_001010983.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1638,
"cdna_end": null,
"cdna_length": 2085,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001010983.3"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "NM_001278280.2",
"protein_id": "NP_001265209.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1634,
"cdna_end": null,
"cdna_length": 2081,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001278280.2"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "NM_001278281.2",
"protein_id": "NP_001265210.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1382,
"cdna_end": null,
"cdna_length": 1829,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001278281.2"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "NM_152932.3",
"protein_id": "NP_690909.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1259,
"cdna_end": null,
"cdna_length": 1706,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_152932.3"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000491606.5",
"protein_id": "ENSP00000418853.1",
"transcript_support_level": 5,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1147,
"cdna_end": null,
"cdna_length": 1577,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000491606.5"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858361.1",
"protein_id": "ENSP00000528420.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1906,
"cdna_end": null,
"cdna_length": 2686,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858361.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858362.1",
"protein_id": "ENSP00000528421.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1266,
"cdna_end": null,
"cdna_length": 1709,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858362.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858363.1",
"protein_id": "ENSP00000528422.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1282,
"cdna_end": null,
"cdna_length": 2058,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858363.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858364.1",
"protein_id": "ENSP00000528423.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1295,
"cdna_end": null,
"cdna_length": 2064,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858364.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858365.1",
"protein_id": "ENSP00000528424.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1805,
"cdna_end": null,
"cdna_length": 2254,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858365.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858367.1",
"protein_id": "ENSP00000528426.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1817,
"cdna_end": null,
"cdna_length": 2258,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858367.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 13,
"exon_rank_end": null,
"exon_count": 13,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858368.1",
"protein_id": "ENSP00000528427.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 2120,
"cdna_end": null,
"cdna_length": 2567,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858368.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858370.1",
"protein_id": "ENSP00000528429.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1763,
"cdna_end": null,
"cdna_length": 2206,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858370.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858371.1",
"protein_id": "ENSP00000528430.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
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"cds_start": 1028,
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"cdna_start": 1471,
"cdna_end": null,
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"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858371.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858372.1",
"protein_id": "ENSP00000528431.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
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"cdna_start": 1522,
"cdna_end": null,
"cdna_length": 1963,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858372.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 10,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858373.1",
"protein_id": "ENSP00000528432.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
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"cdna_start": 2132,
"cdna_end": null,
"cdna_length": 2579,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858373.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858374.1",
"protein_id": "ENSP00000528433.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
"aa_length": 371,
"cds_start": 1028,
"cds_end": null,
"cds_length": 1116,
"cdna_start": 1581,
"cdna_end": null,
"cdna_length": 2022,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000858374.1"
},
{
"aa_ref": "T",
"aa_alt": "S",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 11,
"exon_rank_end": null,
"exon_count": 11,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "GLT8D1",
"gene_hgnc_id": 24870,
"hgvs_c": "c.1028C>G",
"hgvs_p": "p.Thr343Ser",
"transcript": "ENST00000858375.1",
"protein_id": "ENSP00000528434.1",
"transcript_support_level": null,
"aa_start": 343,
"aa_end": null,
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{
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{
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],
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}
],
"message": null
}