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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: 8-104234890-C-T (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=8&pos=104234890&ref=C&alt=T&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "8",
"pos": 104234890,
"ref": "C",
"alt": "T",
"effect": "intron_variant",
"transcript": "ENST00000696799.1",
"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": 30,
"intron_rank": 25,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.4109-10026C>T",
"hgvs_p": null,
"transcript": "NM_001348484.3",
"protein_id": "NP_001335413.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1607,
"cds_start": -4,
"cds_end": null,
"cds_length": 4824,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7711,
"mane_select": "ENST00000696799.1",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 30,
"intron_rank": 25,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.4109-10026C>T",
"hgvs_p": null,
"transcript": "ENST00000696799.1",
"protein_id": "ENSP00000512879.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1607,
"cds_start": -4,
"cds_end": null,
"cds_length": 4824,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7711,
"mane_select": "NM_001348484.3",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 27,
"intron_rank": 22,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.3356-10026C>T",
"hgvs_p": null,
"transcript": "ENST00000408894.7",
"protein_id": "ENSP00000386228.3",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1356,
"cds_start": -4,
"cds_end": null,
"cds_length": 4071,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6969,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 21,
"intron_rank": 16,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.2852-10026C>T",
"hgvs_p": null,
"transcript": "ENST00000262231.14",
"protein_id": "ENSP00000262231.10",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1188,
"cds_start": -4,
"cds_end": null,
"cds_length": 3567,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 3854,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 22,
"intron_rank": 17,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.2777-10026C>T",
"hgvs_p": null,
"transcript": "ENST00000507740.6",
"protein_id": "ENSP00000423559.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1163,
"cds_start": -4,
"cds_end": null,
"cds_length": 3492,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 6390,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 22,
"intron_rank": 17,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "n.2665-10026C>T",
"hgvs_p": null,
"transcript": "ENST00000515551.6",
"protein_id": "ENSP00000425205.2",
"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": 3657,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 31,
"intron_rank": 26,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.4064-10026C>T",
"hgvs_p": null,
"transcript": "ENST00000666250.1",
"protein_id": "ENSP00000499454.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1592,
"cds_start": -4,
"cds_end": null,
"cds_length": 4779,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 7564,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 30,
"intron_rank": 25,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.3968-10026C>T",
"hgvs_p": null,
"transcript": "NM_001395654.1",
"protein_id": "NP_001382583.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1560,
"cds_start": -4,
"cds_end": null,
"cds_length": 4683,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9234,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"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": 30,
"intron_rank": 25,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.3962-10026C>T",
"hgvs_p": null,
"transcript": "NM_001395652.1",
"protein_id": "NP_001382581.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1558,
"cds_start": -4,
"cds_end": null,
"cds_length": 4677,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 9228,
"mane_select": null,
"mane_plus": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 29,
"intron_rank": 24,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.3935-10026C>T",
"hgvs_p": null,
"transcript": "NM_001348489.2",
"protein_id": "NP_001335418.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1549,
"cds_start": -4,
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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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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 27,
"intron_rank": 22,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.3851-10026C>T",
"hgvs_p": null,
"transcript": "ENST00000705945.1",
"protein_id": "ENSP00000516182.1",
"transcript_support_level": null,
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},
{
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"strand": true,
"consequences": [
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],
"exon_rank": null,
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"intron_rank": 23,
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"gene_symbol": "RIMS2",
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"hgvs_c": "c.3848-10026C>T",
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"transcript": "NM_001348490.2",
"protein_id": "NP_001335419.1",
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},
{
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"strand": true,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 30,
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"gene_symbol": "RIMS2",
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"hgvs_c": "c.3821-10026C>T",
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"transcript": "NM_001395653.1",
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},
{
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],
"exon_rank": null,
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"gene_symbol": "RIMS2",
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"hgvs_c": "c.3737-10026C>T",
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},
{
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],
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"gene_symbol": "RIMS2",
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"hgvs_c": "c.3656-10026C>T",
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"transcript": "ENST00000705942.1",
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},
{
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],
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"gene_symbol": "RIMS2",
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"hgvs_c": "c.3623-10026C>T",
"hgvs_p": null,
"transcript": "ENST00000705946.1",
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],
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"hgvs_c": "c.3590-10026C>T",
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"transcript": "ENST00000668113.1",
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},
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],
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"intron_rank": 20,
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"gene_symbol": "RIMS2",
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"hgvs_c": "c.3548-10026C>T",
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"transcript": "NM_001348491.2",
"protein_id": "NP_001335420.1",
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],
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"gene_symbol": "RIMS2",
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"hgvs_c": "c.3506-10026C>T",
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],
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"hgvs_c": "c.3494-10026C>T",
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},
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],
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},
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"consequences": [
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],
"exon_rank": null,
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"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.3419-10026C>T",
"hgvs_p": null,
"transcript": "NM_001348488.2",
"protein_id": "NP_001335417.1",
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},
{
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"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 25,
"intron_rank": 20,
"intron_rank_end": null,
"gene_symbol": "RIMS2",
"gene_hgnc_id": 17283,
"hgvs_c": "c.3410-10026C>T",
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"transcript": "ENST00000705941.1",
"protein_id": "ENSP00000516178.1",
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