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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: 15-40303426-G-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=15&pos=40303426&ref=G&alt=A&genome=hg38&allGenes=true"
API Response
json
{
"variants": [
{
"chr": "15",
"pos": 40303426,
"ref": "G",
"alt": "A",
"effect": "intron_variant",
"transcript": "ENST00000260402.8",
"consequences": [
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "NM_004573.3",
"protein_id": "NP_004564.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1185,
"cds_start": -4,
"cds_end": null,
"cds_length": 3558,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4627,
"mane_select": "ENST00000260402.8",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "ENST00000260402.8",
"protein_id": "ENSP00000260402.3",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 1185,
"cds_start": -4,
"cds_end": null,
"cds_length": 3558,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4627,
"mane_select": "NM_004573.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "ENST00000557821.5",
"protein_id": "ENSP00000453975.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1181,
"cds_start": -4,
"cds_end": null,
"cds_length": 3546,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4517,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "ENST00000456256.6",
"protein_id": "ENSP00000411991.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1170,
"cds_start": -4,
"cds_end": null,
"cds_length": 3513,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4242,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "ENST00000543785.3",
"protein_id": "ENSP00000444652.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 199,
"cds_start": -4,
"cds_end": null,
"cds_length": 600,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1763,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 32,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "NM_001284297.2",
"protein_id": "NP_001271226.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1181,
"cds_start": -4,
"cds_end": null,
"cds_length": 3546,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4615,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "NM_001284298.2",
"protein_id": "NP_001271227.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1170,
"cds_start": -4,
"cds_end": null,
"cds_length": 3513,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4582,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 8,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "NM_001284299.2",
"protein_id": "NP_001271228.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 199,
"cds_start": -4,
"cds_end": null,
"cds_length": 600,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 1788,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 29,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "n.184-70C>T",
"hgvs_p": null,
"transcript": "ENST00000558588.5",
"protein_id": null,
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": null,
"cds_start": -4,
"cds_end": null,
"cds_length": null,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4643,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "XM_017022314.3",
"protein_id": "XP_016877803.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1205,
"cds_start": -4,
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"cds_length": 3618,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4687,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "XM_047432667.1",
"protein_id": "XP_047288623.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1204,
"cds_start": -4,
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"cdna_start": null,
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"mane_select": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 33,
"intron_rank": 2,
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"gene_symbol": "PLCB2",
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"hgvs_c": "c.163-70C>T",
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"transcript": "XM_047432668.1",
"protein_id": "XP_047288624.1",
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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": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 33,
"intron_rank": 2,
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"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "XM_017022317.3",
"protein_id": "XP_016877806.1",
"transcript_support_level": null,
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{
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],
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"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "XM_047432669.1",
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},
{
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"consequences": [
"intron_variant"
],
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"gene_symbol": "PLCB2",
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"transcript": "XM_047432670.1",
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"feature": null
},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 32,
"intron_rank": 2,
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"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "XM_047432671.1",
"protein_id": "XP_047288627.1",
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},
{
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],
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"gene_symbol": "PLCB2",
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"hgvs_c": "c.163-70C>T",
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"transcript": "XM_047432672.1",
"protein_id": "XP_047288628.1",
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"feature": null
},
{
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"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 32,
"intron_rank": 2,
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"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "XM_047432673.1",
"protein_id": "XP_047288629.1",
"transcript_support_level": null,
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 32,
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"gene_symbol": "PLCB2",
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"hgvs_c": "c.163-70C>T",
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"transcript": "XM_047432674.1",
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},
{
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],
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"gene_symbol": "PLCB2",
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"hgvs_c": "c.163-70C>T",
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"transcript": "XM_047432675.1",
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],
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"intron_rank": 2,
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"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
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"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "XM_047432677.1",
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"cdna_start": null,
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"mane_select": null,
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"biotype": null,
"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 31,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "PLCB2",
"gene_hgnc_id": 9055,
"hgvs_c": "c.163-70C>T",
"hgvs_p": null,
"transcript": "XM_047432678.1",
"protein_id": "XP_047288634.1",
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