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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: 9-35343559-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=9&pos=35343559&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "9",
"pos": 35343559,
"ref": "C",
"alt": "G",
"effect": "intron_variant",
"transcript": "NM_001371189.2",
"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": 40,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "UNC13B",
"gene_hgnc_id": 12566,
"hgvs_c": "c.9415-23388C>G",
"hgvs_p": null,
"transcript": "NM_001371189.2",
"protein_id": "NP_001358118.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 4340,
"cds_start": null,
"cds_end": null,
"cds_length": 13023,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 14600,
"mane_select": "ENST00000635942.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001371189.2"
},
{
"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": 40,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "UNC13B",
"gene_hgnc_id": 12566,
"hgvs_c": "c.9415-23388C>G",
"hgvs_p": null,
"transcript": "ENST00000635942.2",
"protein_id": "ENSP00000490228.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 4340,
"cds_start": null,
"cds_end": null,
"cds_length": 13023,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 14600,
"mane_select": "NM_001371189.2",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000635942.2"
},
{
"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": 40,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "UNC13B",
"gene_hgnc_id": 12566,
"hgvs_c": "c.1168-23388C>G",
"hgvs_p": null,
"transcript": "ENST00000619578.4",
"protein_id": "ENSP00000479261.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1610,
"cds_start": null,
"cds_end": null,
"cds_length": 4833,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6426,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000619578.4"
},
{
"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": 39,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "UNC13B",
"gene_hgnc_id": 12566,
"hgvs_c": "c.1168-23388C>G",
"hgvs_p": null,
"transcript": "ENST00000378495.7",
"protein_id": "ENSP00000367756.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1591,
"cds_start": null,
"cds_end": null,
"cds_length": 4776,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6303,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000378495.7"
},
{
"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": 33,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "UNC13B",
"gene_hgnc_id": 12566,
"hgvs_c": "c.-234+1215C>G",
"hgvs_p": null,
"transcript": "NM_001371187.2",
"protein_id": "NP_001358116.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1990,
"cds_start": null,
"cds_end": null,
"cds_length": 5973,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7957,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001371187.2"
},
{
"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": 33,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "UNC13B",
"gene_hgnc_id": 12566,
"hgvs_c": "c.-234+1215C>G",
"hgvs_p": null,
"transcript": "ENST00000636694.1",
"protein_id": "ENSP00000490683.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 1990,
"cds_start": null,
"cds_end": null,
"cds_length": 5973,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 8012,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000636694.1"
},
{
"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": 33,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "UNC13B",
"gene_hgnc_id": 12566,
"hgvs_c": "c.-234+1215C>G",
"hgvs_p": null,
"transcript": "NM_001387555.1",
"protein_id": "NP_001374484.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1989,
"cds_start": null,
"cds_end": null,
"cds_length": 5970,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7954,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001387555.1"
},
{
"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": 39,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "UNC13B",
"gene_hgnc_id": 12566,
"hgvs_c": "c.1168-23388C>G",
"hgvs_p": null,
"transcript": "ENST00000893383.1",
"protein_id": "ENSP00000563442.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1629,
"cds_start": null,
"cds_end": null,
"cds_length": 4890,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6518,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000893383.1"
},
{
"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": 41,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "UNC13B",
"gene_hgnc_id": 12566,
"hgvs_c": "c.1204-23388C>G",
"hgvs_p": null,
"transcript": "ENST00000396787.5",
"protein_id": "ENSP00000380006.1",
"transcript_support_level": 5,
"aa_start": null,
"aa_end": null,
"aa_length": 1622,
"cds_start": null,
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"cds_length": 4869,
"cdna_start": null,
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"cdna_length": 5293,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000396787.5"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 40,
"intron_rank": 11,
"intron_rank_end": null,
"gene_symbol": "UNC13B",
"gene_hgnc_id": 12566,
"hgvs_c": "c.1261-23388C>G",
"hgvs_p": null,
"transcript": "ENST00000893388.1",
"protein_id": "ENSP00000563447.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": 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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"biotype": "protein_coding",
"feature": "ENST00000893388.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 40,
"intron_rank": 10,
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"gene_symbol": "UNC13B",
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"hgvs_c": "c.1168-23388C>G",
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"transcript": "NM_001330653.3",
"protein_id": "NP_001317582.1",
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},
{
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"consequences": [
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],
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"gene_symbol": "UNC13B",
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"hgvs_c": "c.1204-23388C>G",
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"transcript": "NM_001387551.1",
"protein_id": "NP_001374480.1",
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},
{
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"strand": true,
"consequences": [
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],
"exon_rank": null,
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"gene_symbol": "UNC13B",
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"transcript": "ENST00000893382.1",
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},
{
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],
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},
{
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],
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"exon_count": 39,
"intron_rank": 10,
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"gene_symbol": "UNC13B",
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"hgvs_c": "c.1168-23388C>G",
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"transcript": "NM_001371186.2",
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},
{
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],
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},
{
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],
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"gene_symbol": "UNC13B",
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"hgvs_c": "c.1168-23388C>G",
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"transcript": "ENST00000926709.1",
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},
{
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"strand": true,
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],
"exon_rank": null,
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"exon_count": 39,
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"gene_symbol": "UNC13B",
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"hgvs_c": "c.1159-23388C>G",
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"transcript": "ENST00000893385.1",
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},
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],
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"intron_rank": 9,
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"gene_symbol": "UNC13B",
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},
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],
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},
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],
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"gene_symbol": "UNC13B",
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"hgvs_c": "c.1168-23388C>G",
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"transcript": "ENST00000893386.1",
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"biotype": "protein_coding",
"feature": "ENST00000893386.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 37,
"intron_rank": 10,
"intron_rank_end": null,
"gene_symbol": "UNC13B",
"gene_hgnc_id": 12566,
"hgvs_c": "c.1167+29570C>G",
"hgvs_p": null,
"transcript": "ENST00000893387.1",
"protein_id": "ENSP00000563446.1",
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"aa_start": null,
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"mane_select": null,
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},
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