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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: 5-170996530-C-G (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=5&pos=170996530&ref=C&alt=G&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "5",
"pos": 170996530,
"ref": "C",
"alt": "G",
"effect": "intron_variant",
"transcript": "ENST00000523189.6",
"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": 28,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "c.1710+28153C>G",
"hgvs_p": null,
"transcript": "NM_022897.5",
"protein_id": "NP_075048.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1088,
"cds_start": -4,
"cds_end": null,
"cds_length": 3267,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4440,
"mane_select": "ENST00000523189.6",
"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": 28,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "c.1710+28153C>G",
"hgvs_p": null,
"transcript": "ENST00000523189.6",
"protein_id": "ENSP00000427975.1",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 1088,
"cds_start": -4,
"cds_end": null,
"cds_length": 3267,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 4440,
"mane_select": "NM_022897.5",
"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": 30,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "n.1710+28153C>G",
"hgvs_p": null,
"transcript": "ENST00000389118.8",
"protein_id": "ENSP00000373770.4",
"transcript_support_level": 2,
"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": 3653,
"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": 3,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "n.120+28153C>G",
"hgvs_p": null,
"transcript": "ENST00000518492.1",
"protein_id": "ENSP00000427980.1",
"transcript_support_level": 2,
"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": 296,
"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": 27,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "n.1710+28153C>G",
"hgvs_p": null,
"transcript": "ENST00000519256.5",
"protein_id": "ENSP00000429298.1",
"transcript_support_level": 2,
"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": 3375,
"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": 30,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "n.1710+28153C>G",
"hgvs_p": null,
"transcript": "ENST00000519949.5",
"protein_id": "ENSP00000430444.1",
"transcript_support_level": 2,
"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": 4618,
"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": 20,
"intron_rank": 13,
"intron_rank_end": null,
"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "n.1641+28153C>G",
"hgvs_p": null,
"transcript": "ENST00000520864.5",
"protein_id": "ENSP00000429845.1",
"transcript_support_level": 2,
"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": 4573,
"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": 30,
"intron_rank": 15,
"intron_rank_end": null,
"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "n.*148+13285C>G",
"hgvs_p": null,
"transcript": "ENST00000522066.5",
"protein_id": "ENSP00000430958.1",
"transcript_support_level": 2,
"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": 4739,
"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": 29,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "n.1710+28153C>G",
"hgvs_p": null,
"transcript": "ENST00000522533.5",
"protein_id": "ENSP00000430599.1",
"transcript_support_level": 2,
"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": 4558,
"mane_select": null,
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": true,
"strand": true,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 28,
"intron_rank": 14,
"intron_rank_end": null,
"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "c.1710+28153C>G",
"hgvs_p": null,
"transcript": "XM_011534627.2",
"protein_id": "XP_011532929.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 1092,
"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": 13,
"intron_rank_end": null,
"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "c.1590+28153C>G",
"hgvs_p": null,
"transcript": "XM_017009736.2",
"protein_id": "XP_016865225.1",
"transcript_support_level": null,
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"cds_start": -4,
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},
{
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"strand": true,
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],
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"gene_symbol": "RANBP17",
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"hgvs_c": "c.1590+28153C>G",
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"transcript": "XM_047417530.1",
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},
{
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"consequences": [
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],
"exon_rank": null,
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"exon_count": 27,
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"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "c.1563+28153C>G",
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"transcript": "XM_017009738.2",
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},
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],
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"gene_symbol": "RANBP17",
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"hgvs_c": "c.1563+28153C>G",
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},
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],
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},
{
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],
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"transcript": "XM_017009741.3",
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],
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},
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],
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"gene_symbol": "RANBP17",
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"hgvs_c": "c.810+28153C>G",
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"transcript": "XM_017009745.2",
"protein_id": "XP_016865234.1",
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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": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "c.1710+28153C>G",
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"transcript": "XM_011534636.3",
"protein_id": "XP_011532938.1",
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"mane_select": null,
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},
{
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"protein_coding": true,
"strand": true,
"consequences": [
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],
"exon_rank": null,
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"exon_count": 15,
"intron_rank": 14,
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"gene_symbol": "RANBP17",
"gene_hgnc_id": 14428,
"hgvs_c": "c.1711-27961C>G",
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"transcript": "XM_011534637.3",
"protein_id": "XP_011532939.1",
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],
"clinvar_disease": "",
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}
],
"message": null
}