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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: 12-88107031-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=12&pos=88107031&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "12",
"pos": 88107031,
"ref": "C",
"alt": "T",
"effect": "missense_variant",
"transcript": "ENST00000552810.6",
"consequences": [
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.2551G>A",
"hgvs_p": "p.Val851Ile",
"transcript": "NM_025114.4",
"protein_id": "NP_079390.3",
"transcript_support_level": null,
"aa_start": 851,
"aa_end": null,
"aa_length": 2479,
"cds_start": 2551,
"cds_end": null,
"cds_length": 7440,
"cdna_start": 2767,
"cdna_end": null,
"cdna_length": 7824,
"mane_select": "ENST00000552810.6",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": true,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 54,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.2551G>A",
"hgvs_p": "p.Val851Ile",
"transcript": "ENST00000552810.6",
"protein_id": "ENSP00000448012.1",
"transcript_support_level": 1,
"aa_start": 851,
"aa_end": null,
"aa_length": 2479,
"cds_start": 2551,
"cds_end": null,
"cds_length": 7440,
"cdna_start": 2767,
"cdna_end": null,
"cdna_length": 7824,
"mane_select": "NM_025114.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 16,
"exon_rank_end": null,
"exon_count": 20,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.1810G>A",
"hgvs_p": "p.Val604Ile",
"transcript": "ENST00000604024.5",
"protein_id": "ENSP00000473863.1",
"transcript_support_level": 1,
"aa_start": 604,
"aa_end": null,
"aa_length": 857,
"cds_start": 1810,
"cds_end": null,
"cds_length": 2574,
"cdna_start": 1810,
"cdna_end": null,
"cdna_length": 2741,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 56,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.3412G>A",
"hgvs_p": "p.Val1138Ile",
"transcript": "ENST00000675476.1",
"protein_id": "ENSP00000502161.1",
"transcript_support_level": null,
"aa_start": 1138,
"aa_end": null,
"aa_length": 2766,
"cds_start": 3412,
"cds_end": null,
"cds_length": 8301,
"cdna_start": 3639,
"cdna_end": null,
"cdna_length": 8696,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.3319G>A",
"hgvs_p": "p.Val1107Ile",
"transcript": "ENST00000675833.1",
"protein_id": "ENSP00000502559.1",
"transcript_support_level": null,
"aa_start": 1107,
"aa_end": null,
"aa_length": 2735,
"cds_start": 3319,
"cds_end": null,
"cds_length": 8208,
"cdna_start": 3546,
"cdna_end": null,
"cdna_length": 8603,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 55,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.2551G>A",
"hgvs_p": "p.Val851Ile",
"transcript": "ENST00000309041.12",
"protein_id": "ENSP00000308021.8",
"transcript_support_level": 5,
"aa_start": 851,
"aa_end": null,
"aa_length": 2482,
"cds_start": 2551,
"cds_end": null,
"cds_length": 7449,
"cdna_start": 2778,
"cdna_end": null,
"cdna_length": 7844,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 23,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.2530G>A",
"hgvs_p": "p.Val844Ile",
"transcript": "ENST00000675230.1",
"protein_id": "ENSP00000502503.1",
"transcript_support_level": null,
"aa_start": 844,
"aa_end": null,
"aa_length": 2472,
"cds_start": 2530,
"cds_end": null,
"cds_length": 7419,
"cdna_start": 2757,
"cdna_end": null,
"cdna_length": 7814,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.2551G>A",
"hgvs_p": "p.Val851Ile",
"transcript": "ENST00000673058.2",
"protein_id": "ENSP00000500665.2",
"transcript_support_level": null,
"aa_start": 851,
"aa_end": null,
"aa_length": 2438,
"cds_start": 2551,
"cds_end": null,
"cds_length": 7317,
"cdna_start": 2778,
"cdna_end": null,
"cdna_length": 7712,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 24,
"exon_rank_end": null,
"exon_count": 53,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.2551G>A",
"hgvs_p": "p.Val851Ile",
"transcript": "ENST00000675408.1",
"protein_id": "ENSP00000502298.1",
"transcript_support_level": null,
"aa_start": 851,
"aa_end": null,
"aa_length": 2424,
"cds_start": 2551,
"cds_end": null,
"cds_length": 7275,
"cdna_start": 2778,
"cdna_end": null,
"cdna_length": 7670,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.3412G>A",
"hgvs_p": "p.Val1138Ile",
"transcript": "XM_011538756.4",
"protein_id": "XP_011537058.1",
"transcript_support_level": null,
"aa_start": 1138,
"aa_end": null,
"aa_length": 2769,
"cds_start": 3412,
"cds_end": null,
"cds_length": 8310,
"cdna_start": 3628,
"cdna_end": null,
"cdna_length": 8694,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.3412G>A",
"hgvs_p": "p.Val1138Ile",
"transcript": "XM_011538757.4",
"protein_id": "XP_011537059.1",
"transcript_support_level": null,
"aa_start": 1138,
"aa_end": null,
"aa_length": 2769,
"cds_start": 3412,
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"cds_length": 8310,
"cdna_start": 3566,
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"cdna_length": 8632,
"mane_select": null,
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"feature": null
},
{
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"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 57,
"intron_rank": null,
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"gene_symbol": "CEP290",
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"hgvs_c": "c.3412G>A",
"hgvs_p": "p.Val1138Ile",
"transcript": "XM_011538758.4",
"protein_id": "XP_011537060.1",
"transcript_support_level": null,
"aa_start": 1138,
"aa_end": null,
"aa_length": 2768,
"cds_start": 3412,
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"cdna_start": 3628,
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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": [
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],
"exon_rank": 26,
"exon_rank_end": null,
"exon_count": 56,
"intron_rank": null,
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"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.3412G>A",
"hgvs_p": "p.Val1138Ile",
"transcript": "XM_011538759.3",
"protein_id": "XP_011537061.1",
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"aa_length": 2766,
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"cdna_start": 3628,
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},
{
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],
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"intron_rank": null,
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"gene_symbol": "CEP290",
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"transcript": "XM_011538760.3",
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},
{
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],
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"intron_rank": null,
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"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.3412G>A",
"hgvs_p": "p.Val1138Ile",
"transcript": "XM_017019980.3",
"protein_id": "XP_016875469.1",
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"aa_start": 1138,
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},
{
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],
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"exon_count": 56,
"intron_rank": null,
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"gene_symbol": "CEP290",
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"hgvs_c": "c.3412G>A",
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"transcript": "XM_011538761.3",
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},
{
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],
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"exon_count": 55,
"intron_rank": null,
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"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.3412G>A",
"hgvs_p": "p.Val1138Ile",
"transcript": "XM_017019981.3",
"protein_id": "XP_016875470.1",
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},
{
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"strand": false,
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],
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"exon_count": 54,
"intron_rank": null,
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"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.3412G>A",
"hgvs_p": "p.Val1138Ile",
"transcript": "XM_017019982.2",
"protein_id": "XP_016875471.1",
"transcript_support_level": null,
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},
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"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
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"hgvs_p": "p.Val1138Ile",
"transcript": "XM_047429558.1",
"protein_id": "XP_047285514.1",
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},
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"intron_rank": null,
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"gene_symbol": "CEP290",
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},
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"gene_symbol": "CEP290",
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"hgvs_p": "p.Val882Ile",
"transcript": "XM_011538762.4",
"protein_id": "XP_011537064.1",
"transcript_support_level": null,
"aa_start": 882,
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"cds_start": 2644,
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"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 56,
"intron_rank": null,
"intron_rank_end": null,
"gene_symbol": "CEP290",
"gene_hgnc_id": 29021,
"hgvs_c": "c.2644G>A",
"hgvs_p": "p.Val882Ile",
"transcript": "XM_047429560.1",
"protein_id": "XP_047285516.1",
"transcript_support_level": null,
"aa_start": 882,
"aa_end": null,
"aa_length": 2513,
"cds_start": 2644,
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"cdna_start": 2813,
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"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": "V",
"aa_alt": "I",
"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"missense_variant"
],
"exon_rank": 25,
"exon_rank_end": null,
"exon_count": 55,
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}