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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: 2-229844482-A-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=229844482&ref=A&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "2",
"pos": 229844482,
"ref": "A",
"alt": "G",
"effect": "intron_variant",
"transcript": "ENST00000675903.1",
"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": 42,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TRIP12",
"gene_hgnc_id": 12306,
"hgvs_c": "c.1028-3555T>C",
"hgvs_p": null,
"transcript": "NM_001348323.3",
"protein_id": "NP_001335252.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2067,
"cds_start": -4,
"cds_end": null,
"cds_length": 6204,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10100,
"mane_select": "ENST00000675903.1",
"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": 42,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TRIP12",
"gene_hgnc_id": 12306,
"hgvs_c": "c.1028-3555T>C",
"hgvs_p": null,
"transcript": "ENST00000675903.1",
"protein_id": "ENSP00000502713.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2067,
"cds_start": -4,
"cds_end": null,
"cds_length": 6204,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10100,
"mane_select": "NM_001348323.3",
"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": 42,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TRIP12",
"gene_hgnc_id": 12306,
"hgvs_c": "c.1028-3555T>C",
"hgvs_p": null,
"transcript": "ENST00000389044.8",
"protein_id": "ENSP00000373696.4",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 2040,
"cds_start": -4,
"cds_end": null,
"cds_length": 6123,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6405,
"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": 41,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "TRIP12",
"gene_hgnc_id": 12306,
"hgvs_c": "c.902-3555T>C",
"hgvs_p": null,
"transcript": "ENST00000283943.9",
"protein_id": "ENSP00000283943.4",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1992,
"cds_start": -4,
"cds_end": null,
"cds_length": 5979,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9874,
"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": 39,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "TRIP12",
"gene_hgnc_id": 12306,
"hgvs_c": "c.99-7498T>C",
"hgvs_p": null,
"transcript": "ENST00000389045.7",
"protein_id": "ENSP00000373697.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1722,
"cds_start": -4,
"cds_end": null,
"cds_length": 5169,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 5355,
"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": 16,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "TRIP12",
"gene_hgnc_id": 12306,
"hgvs_c": "n.1081-3555T>C",
"hgvs_p": null,
"transcript": "ENST00000479037.5",
"protein_id": null,
"transcript_support_level": 1,
"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": 2938,
"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": 42,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TRIP12",
"gene_hgnc_id": 12306,
"hgvs_c": "c.1028-3555T>C",
"hgvs_p": null,
"transcript": "NM_001348328.1",
"protein_id": "NP_001335257.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2068,
"cds_start": -4,
"cds_end": null,
"cds_length": 6207,
"cdna_start": null,
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"cdna_length": 10103,
"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": 42,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TRIP12",
"gene_hgnc_id": 12306,
"hgvs_c": "c.1028-3555T>C",
"hgvs_p": null,
"transcript": "NM_001348329.2",
"protein_id": "NP_001335258.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2068,
"cds_start": -4,
"cds_end": null,
"cds_length": 6207,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 10454,
"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": 42,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TRIP12",
"gene_hgnc_id": 12306,
"hgvs_c": "c.1028-3555T>C",
"hgvs_p": null,
"transcript": "NM_001348330.2",
"protein_id": "NP_001335259.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 2068,
"cds_start": -4,
"cds_end": null,
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"cdna_start": null,
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"cdna_length": 10492,
"mane_select": null,
"mane_plus": null,
"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": 42,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "TRIP12",
"gene_hgnc_id": 12306,
"hgvs_c": "c.1028-3555T>C",
"hgvs_p": null,
"transcript": "ENST00000675453.1",
"protein_id": "ENSP00000502271.1",
"transcript_support_level": null,
"aa_start": null,
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"cds_start": -4,
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"biotype": null,
"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": 43,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "TRIP12",
"gene_hgnc_id": 12306,
"hgvs_c": "c.1028-3555T>C",
"hgvs_p": null,
"transcript": "NM_001348322.1",
"protein_id": "NP_001335251.1",
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},
{
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"protein_coding": true,
"strand": false,
"consequences": [
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],
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"gene_symbol": "TRIP12",
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"transcript": "NM_001348324.2",
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},
{
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],
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"gene_symbol": "TRIP12",
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"hgvs_c": "c.1028-3555T>C",
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"transcript": "NM_001348325.2",
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},
{
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],
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"gene_symbol": "TRIP12",
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"hgvs_c": "c.1028-3555T>C",
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},
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],
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"hgvs_c": "c.1028-3555T>C",
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"transcript": "NM_001348327.2",
"protein_id": "NP_001335256.1",
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},
{
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],
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"gene_symbol": "TRIP12",
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],
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"gene_symbol": "TRIP12",
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},
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],
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"gene_symbol": "TRIP12",
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"hgvs_c": "c.1028-3555T>C",
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"transcript": "NM_001348321.1",
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},
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],
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"intron_rank": 3,
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"gene_symbol": "TRIP12",
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"consequences": [
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],
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"gene_symbol": "TRIP12",
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"hgvs_c": "c.1028-3555T>C",
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"transcript": "NM_001348333.1",
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},
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"consequences": [
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],
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"gene_symbol": "TRIP12",
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"hgvs_c": "c.1028-3555T>C",
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}