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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: 11-8777306-G-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=11&pos=8777306&ref=G&alt=C&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "11",
"pos": 8777306,
"ref": "G",
"alt": "C",
"effect": "intron_variant",
"transcript": "ENST00000313726.11",
"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": 20,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "DENND2B",
"gene_hgnc_id": 11350,
"hgvs_c": "c.-25-26581C>G",
"hgvs_p": null,
"transcript": "NM_213618.2",
"protein_id": "NP_998783.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1137,
"cds_start": -4,
"cds_end": null,
"cds_length": 3414,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4341,
"mane_select": "ENST00000313726.11",
"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": 20,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "DENND2B",
"gene_hgnc_id": 11350,
"hgvs_c": "c.-25-26581C>G",
"hgvs_p": null,
"transcript": "ENST00000313726.11",
"protein_id": "ENSP00000319678.6",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1137,
"cds_start": -4,
"cds_end": null,
"cds_length": 3414,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4341,
"mane_select": "NM_213618.2",
"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": 23,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "DENND2B",
"gene_hgnc_id": 11350,
"hgvs_c": "c.-25-26581C>G",
"hgvs_p": null,
"transcript": "ENST00000534127.5",
"protein_id": "ENSP00000433528.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1137,
"cds_start": -4,
"cds_end": null,
"cds_length": 3414,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4545,
"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": 19,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "DENND2B",
"gene_hgnc_id": 11350,
"hgvs_c": "c.-25-26581C>G",
"hgvs_p": null,
"transcript": "ENST00000526757.5",
"protein_id": "ENSP00000435097.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 717,
"cds_start": -4,
"cds_end": null,
"cds_length": 2154,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3019,
"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": 19,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "DENND2B",
"gene_hgnc_id": 11350,
"hgvs_c": "c.-25-26581C>G",
"hgvs_p": null,
"transcript": "ENST00000530438.5",
"protein_id": "ENSP00000436802.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 717,
"cds_start": -4,
"cds_end": null,
"cds_length": 2154,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2679,
"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": 24,
"intron_rank": 5,
"intron_rank_end": null,
"gene_symbol": "DENND2B",
"gene_hgnc_id": 11350,
"hgvs_c": "c.-25-26581C>G",
"hgvs_p": null,
"transcript": "NM_001376495.1",
"protein_id": "NP_001363424.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1137,
"cds_start": -4,
"cds_end": null,
"cds_length": 3414,
"cdna_start": null,
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"cdna_length": 4617,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "DENND2B",
"gene_hgnc_id": 11350,
"hgvs_c": "c.-25-26581C>G",
"hgvs_p": null,
"transcript": "NM_001376496.1",
"protein_id": "NP_001363425.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1137,
"cds_start": -4,
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"cdna_start": null,
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"cdna_length": 4443,
"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": 21,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "DENND2B",
"gene_hgnc_id": 11350,
"hgvs_c": "c.-25-26581C>G",
"hgvs_p": null,
"transcript": "NM_001376497.1",
"protein_id": "NP_001363426.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1137,
"cds_start": -4,
"cds_end": null,
"cds_length": 3414,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4340,
"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": 23,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "DENND2B",
"gene_hgnc_id": 11350,
"hgvs_c": "c.-25-26581C>G",
"hgvs_p": null,
"transcript": "NM_005418.4",
"protein_id": "NP_005409.3",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1137,
"cds_start": -4,
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"cds_length": 3414,
"cdna_start": null,
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"mane_select": null,
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},
{
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"intron_variant"
],
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"intron_rank": 1,
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"gene_symbol": "DENND2B",
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"hgvs_c": "c.-25-26581C>G",
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"transcript": "NM_001376498.1",
"protein_id": "NP_001363427.1",
"transcript_support_level": null,
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},
{
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"strand": false,
"consequences": [
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],
"exon_rank": null,
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"gene_symbol": "DENND2B",
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"hgvs_c": "c.-461+33211C>G",
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"transcript": "NM_001376499.1",
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},
{
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],
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},
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],
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"gene_symbol": "DENND2B",
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},
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],
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"gene_symbol": "DENND2B",
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},
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],
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},
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},
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],
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"gene_symbol": "DENND2B",
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"hgvs_c": "c.-25-26581C>G",
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},
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],
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"gene_symbol": "DENND2B",
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"hgvs_c": "c.-25-26581C>G",
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}