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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: 5-102831450-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=102831450&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 102831450,
"ref": "C",
"alt": "A",
"effect": "intron_variant",
"transcript": "ENST00000438793.8",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PAM",
"gene_hgnc_id": 8596,
"hgvs_c": "c.-373-34373C>A",
"hgvs_p": null,
"transcript": "NM_001177306.2",
"protein_id": "NP_001170777.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 973,
"cds_start": -4,
"cds_end": null,
"cds_length": 2922,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3990,
"mane_select": "ENST00000438793.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PAM",
"gene_hgnc_id": 8596,
"hgvs_c": "c.-373-34373C>A",
"hgvs_p": null,
"transcript": "ENST00000438793.8",
"protein_id": "ENSP00000396493.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 973,
"cds_start": -4,
"cds_end": null,
"cds_length": 2922,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3990,
"mane_select": "NM_001177306.2",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PAM",
"gene_hgnc_id": 8596,
"hgvs_c": "c.-373-34373C>A",
"hgvs_p": null,
"transcript": "ENST00000304400.12",
"protein_id": "ENSP00000306100.8",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 973,
"cds_start": -4,
"cds_end": null,
"cds_length": 2922,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3832,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PAM",
"gene_hgnc_id": 8596,
"hgvs_c": "c.-373-34373C>A",
"hgvs_p": null,
"transcript": "ENST00000455264.7",
"protein_id": "ENSP00000403461.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 905,
"cds_start": -4,
"cds_end": null,
"cds_length": 2718,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3430,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 25,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PAM",
"gene_hgnc_id": 8596,
"hgvs_c": "c.-373-34373C>A",
"hgvs_p": null,
"transcript": "ENST00000348126.7",
"protein_id": "ENSP00000314638.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 866,
"cds_start": -4,
"cds_end": null,
"cds_length": 2601,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3649,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 27,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PAM",
"gene_hgnc_id": 8596,
"hgvs_c": "c.-373-34373C>A",
"hgvs_p": null,
"transcript": "NM_001319943.1",
"protein_id": "NP_001306872.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 991,
"cds_start": -4,
"cds_end": null,
"cds_length": 2976,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5955,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PAM",
"gene_hgnc_id": 8596,
"hgvs_c": "c.-373-34373C>A",
"hgvs_p": null,
"transcript": "NM_000919.4",
"protein_id": "NP_000910.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 974,
"cds_start": -4,
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"cds_length": 2925,
"cdna_start": null,
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"cdna_length": 3993,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PAM",
"gene_hgnc_id": 8596,
"hgvs_c": "c.-373-34373C>A",
"hgvs_p": null,
"transcript": "ENST00000684529.1",
"protein_id": "ENSP00000507038.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 974,
"cds_start": -4,
"cds_end": null,
"cds_length": 2925,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3993,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 26,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PAM",
"gene_hgnc_id": 8596,
"hgvs_c": "c.-373-34373C>A",
"hgvs_p": null,
"transcript": "NM_001364583.2",
"protein_id": "NP_001351512.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 973,
"cds_start": -4,
"cds_end": null,
"cds_length": 2922,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5379,
"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 26,
"intron_rank": 1,
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"gene_symbol": "PAM",
"gene_hgnc_id": 8596,
"hgvs_c": "c.-373-34373C>A",
"hgvs_p": null,
"transcript": "NM_001364584.2",
"protein_id": "NP_001351513.1",
"transcript_support_level": null,
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"cds_start": -4,
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"cdna_start": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 25,
"intron_rank": 1,
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"gene_symbol": "PAM",
"gene_hgnc_id": 8596,
"hgvs_c": "c.-374+23219C>A",
"hgvs_p": null,
"transcript": "NM_001364582.2",
"protein_id": "NP_001351511.1",
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},
{
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],
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},
{
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],
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"gene_symbol": "PAM",
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],
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"gene_symbol": "PAM",
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"hgvs_c": "c.-373-34373C>A",
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],
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},
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],
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},
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"transcript": "NM_001364587.2",
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},
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],
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"gene_symbol": "PAM",
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},
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],
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"gene_symbol": "PAM",
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