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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: 10-73480219-C-A (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=10&pos=73480219&ref=C&alt=A&genome=hg38&allGenes=true"API Response
json
{
"variants": [
{
"chr": "10",
"pos": 73480219,
"ref": "C",
"alt": "A",
"effect": "intron_variant",
"transcript": "NM_001142353.3",
"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": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
"hgvs_p": null,
"transcript": "NM_021132.4",
"protein_id": "NP_066955.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 524,
"cds_start": null,
"cds_end": null,
"cds_length": 1575,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "ENST00000360663.10",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_021132.4"
},
{
"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": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
"hgvs_p": null,
"transcript": "ENST00000360663.10",
"protein_id": "ENSP00000353881.5",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 524,
"cds_start": null,
"cds_end": null,
"cds_length": 1575,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": "NM_021132.4",
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000360663.10"
},
{
"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": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
"hgvs_p": null,
"transcript": "ENST00000394829.6",
"protein_id": "ENSP00000378306.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 525,
"cds_start": null,
"cds_end": null,
"cds_length": 1578,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000394829.6"
},
{
"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": 13,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
"hgvs_p": null,
"transcript": "ENST00000394828.6",
"protein_id": "ENSP00000378305.2",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 515,
"cds_start": null,
"cds_end": null,
"cds_length": 1548,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000394828.6"
},
{
"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": 15,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
"hgvs_p": null,
"transcript": "ENST00000960341.1",
"protein_id": "ENSP00000630400.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 533,
"cds_start": null,
"cds_end": null,
"cds_length": 1602,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960341.1"
},
{
"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": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
"hgvs_p": null,
"transcript": "ENST00000960342.1",
"protein_id": "ENSP00000630401.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 529,
"cds_start": null,
"cds_end": null,
"cds_length": 1590,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960342.1"
},
{
"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": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
"hgvs_p": null,
"transcript": "NM_001142353.3",
"protein_id": "NP_001135825.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 525,
"cds_start": null,
"cds_end": null,
"cds_length": 1578,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "NM_001142353.3"
},
{
"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": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
"hgvs_p": null,
"transcript": "ENST00000885957.1",
"protein_id": "ENSP00000556016.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 523,
"cds_start": null,
"cds_end": null,
"cds_length": 1572,
"cdna_start": null,
"cdna_end": null,
"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000885957.1"
},
{
"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": 14,
"intron_rank": 1,
"intron_rank_end": null,
"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
"hgvs_p": null,
"transcript": "ENST00000960339.1",
"protein_id": "ENSP00000630398.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 522,
"cds_start": null,
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"cds_length": 1569,
"cdna_start": null,
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"cdna_length": null,
"mane_select": null,
"mane_plus": null,
"biotype": "protein_coding",
"feature": "ENST00000960339.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 14,
"intron_rank": 1,
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"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
"hgvs_p": null,
"transcript": "ENST00000885954.1",
"protein_id": "ENSP00000556013.1",
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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": "ENST00000885954.1"
},
{
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"canonical": false,
"protein_coding": true,
"strand": false,
"consequences": [
"intron_variant"
],
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"intron_rank": 1,
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"gene_symbol": "PPP3CB",
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"hgvs_c": "c.86-702G>T",
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"transcript": "ENST00000885955.1",
"protein_id": "ENSP00000556014.1",
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},
{
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],
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"transcript": "NM_001142354.3",
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"biotype": "protein_coding",
"feature": "NM_001142354.3"
},
{
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],
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"gene_symbol": "PPP3CB",
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},
{
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],
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"gene_symbol": "PPP3CB",
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},
{
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],
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"gene_symbol": "PPP3CB",
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"hgvs_c": "c.86-702G>T",
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"transcript": "ENST00000960343.1",
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},
{
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],
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},
{
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],
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"gene_symbol": "PPP3CB",
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"hgvs_c": "c.86-741G>T",
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},
{
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],
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"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
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},
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],
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},
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],
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"feature": "ENST00000960340.1"
},
{
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"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 12,
"intron_rank": 1,
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"gene_symbol": "PPP3CB",
"gene_hgnc_id": 9315,
"hgvs_c": "c.86-702G>T",
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"transcript": "ENST00000925233.1",
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},
{
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"consequences": [
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],
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"intron_rank": 1,
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