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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: 3-138403280-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=3&pos=138403280&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "3",
"pos": 138403280,
"ref": "C",
"alt": "A",
"effect": "3_prime_UTR_variant",
"transcript": "NM_012219.4",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "NM_001085049.3",
"protein_id": "NP_001078518.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 208,
"cds_start": null,
"cds_end": null,
"cds_length": 627,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4098,
"mane_select": "ENST00000423968.7",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001085049.3"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "ENST00000423968.7",
"protein_id": "ENSP00000389682.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 208,
"cds_start": null,
"cds_end": null,
"cds_length": 627,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4098,
"mane_select": "NM_001085049.3",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000423968.7"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "ENST00000949757.1",
"protein_id": "ENSP00000619816.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 216,
"cds_start": null,
"cds_end": null,
"cds_length": 651,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4612,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949757.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "ENST00000949759.1",
"protein_id": "ENSP00000619818.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 216,
"cds_start": null,
"cds_end": null,
"cds_length": 651,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4063,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949759.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "NM_001252090.2",
"protein_id": "NP_001239019.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 208,
"cds_start": null,
"cds_end": null,
"cds_length": 627,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4069,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001252090.2"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "NM_012219.4",
"protein_id": "NP_036351.3",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 208,
"cds_start": null,
"cds_end": null,
"cds_length": 627,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4589,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_012219.4"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 6,
"exon_rank_end": null,
"exon_count": 6,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "ENST00000289104.8",
"protein_id": "ENSP00000289104.4",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 208,
"cds_start": null,
"cds_end": null,
"cds_length": 627,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4538,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000289104.8"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "ENST00000867251.1",
"protein_id": "ENSP00000537310.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 208,
"cds_start": null,
"cds_end": null,
"cds_length": 627,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4505,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000867251.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "ENST00000949756.1",
"protein_id": "ENSP00000619815.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 208,
"cds_start": null,
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"cds_length": 627,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4324,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949756.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "ENST00000949758.1",
"protein_id": "ENSP00000619817.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 208,
"cds_start": null,
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"cds_length": 627,
"cdna_start": null,
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"cdna_length": 4338,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000949758.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
"exon_rank_end": null,
"exon_count": 7,
"intron_rank": null,
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"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "ENST00000949760.1",
"protein_id": "ENSP00000619819.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
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},
{
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"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 8,
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"exon_count": 8,
"intron_rank": null,
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"gene_symbol": "MRAS",
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"transcript": "ENST00000949761.1",
"protein_id": "ENSP00000619820.1",
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"cds_start": null,
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"mane_select": null,
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"feature": "ENST00000949761.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
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"gene_symbol": "MRAS",
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"transcript": "ENST00000949764.1",
"protein_id": "ENSP00000619823.1",
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"cds_start": null,
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"biotype": "protein_coding",
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},
{
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"strand": true,
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],
"exon_rank": 5,
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"gene_symbol": "MRAS",
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"transcript": "NM_001252091.1",
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"biotype": "protein_coding",
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},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
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"exon_count": 5,
"intron_rank": null,
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"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "NM_001252092.2",
"protein_id": "NP_001239021.1",
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"cds_start": null,
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"cdna_start": null,
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"mane_select": null,
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"biotype": "protein_coding",
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},
{
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"protein_coding": true,
"strand": true,
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"3_prime_UTR_variant"
],
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"exon_count": 5,
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"gene_symbol": "MRAS",
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"hgvs_c": "c.*1011C>A",
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"transcript": "NM_001252093.2",
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "NM_001252093.2"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
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"exon_count": 5,
"intron_rank": null,
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"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "ENST00000614350.4",
"protein_id": "ENSP00000484586.1",
"transcript_support_level": 2,
"aa_start": null,
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"cds_start": null,
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"mane_select": null,
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"biotype": "protein_coding",
"feature": "ENST00000614350.4"
},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 5,
"exon_rank_end": null,
"exon_count": 5,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "ENST00000621127.4",
"protein_id": "ENSP00000481637.1",
"transcript_support_level": 5,
"aa_start": null,
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},
{
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"strand": true,
"consequences": [
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],
"exon_rank": 6,
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"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "XM_005247228.2",
"protein_id": "XP_005247285.1",
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"feature": "XM_005247228.2"
},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
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"exon_count": 7,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
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"hgvs_c": "c.*1011C>A",
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"transcript": "XM_024453396.2",
"protein_id": "XP_024309164.1",
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},
{
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"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 7,
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"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "XM_047447695.1",
"protein_id": "XP_047303651.1",
"transcript_support_level": null,
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"cds_start": null,
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"cdna_start": null,
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"cdna_length": 4498,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047447695.1"
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
"exon_rank": 8,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "MRAS",
"gene_hgnc_id": 7227,
"hgvs_c": "c.*1011C>A",
"hgvs_p": null,
"transcript": "XM_047447696.1",
"protein_id": "XP_047303652.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 208,
"cds_start": null,
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"cdna_start": null,
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"cdna_length": 10268,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "XM_047447696.1"
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"3_prime_UTR_variant"
],
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{
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"BS2"
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"clinvar_disease": "",
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}
],
"message": null
}