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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: 2-30967907-A-C (hg38)
Bash / cURL Example
bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=2&pos=30967907&ref=A&alt=C&genome=hg38&allGenes=true"
API Response
json
{
"variants": [
{
"chr": "2",
"pos": 30967907,
"ref": "A",
"alt": "C",
"effect": "intron_variant",
"transcript": "ENST00000349752.10",
"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": 15,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "c.300-1605T>G",
"hgvs_p": null,
"transcript": "NM_024572.4",
"protein_id": "NP_078848.2",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 552,
"cds_start": -4,
"cds_end": null,
"cds_length": 1659,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2447,
"mane_select": "ENST00000349752.10",
"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": 15,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "c.300-1605T>G",
"hgvs_p": null,
"transcript": "ENST00000349752.10",
"protein_id": "ENSP00000288988.6",
"transcript_support_level": 1,
"aa_start": null,
"aa_end": null,
"aa_length": 552,
"cds_start": -4,
"cds_end": null,
"cds_length": 1659,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2447,
"mane_select": "NM_024572.4",
"mane_plus": null,
"biotype": null,
"feature": null
},
{
"aa_ref": null,
"aa_alt": null,
"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 9,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "n.559-1605T>G",
"hgvs_p": null,
"transcript": "ENST00000464038.5",
"protein_id": null,
"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": 991,
"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": 16,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "c.315-1605T>G",
"hgvs_p": null,
"transcript": "NM_001253826.2",
"protein_id": "NP_001240755.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 557,
"cds_start": -4,
"cds_end": null,
"cds_length": 1674,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2462,
"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": 16,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "c.315-1605T>G",
"hgvs_p": null,
"transcript": "ENST00000324589.9",
"protein_id": "ENSP00000314500.5",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 557,
"cds_start": -4,
"cds_end": null,
"cds_length": 1674,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2169,
"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": 17,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "c.240-1605T>G",
"hgvs_p": null,
"transcript": "NM_001253827.2",
"protein_id": "NP_001240756.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 532,
"cds_start": -4,
"cds_end": null,
"cds_length": 1599,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2513,
"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": 17,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "c.240-1605T>G",
"hgvs_p": null,
"transcript": "NM_001329096.2",
"protein_id": "NP_001316025.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 532,
"cds_start": -4,
"cds_end": null,
"cds_length": 1599,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2632,
"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": 17,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "c.240-1605T>G",
"hgvs_p": null,
"transcript": "ENST00000406653.5",
"protein_id": "ENSP00000385435.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 532,
"cds_start": -4,
"cds_end": null,
"cds_length": 1599,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2496,
"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": 16,
"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "c.195-1605T>G",
"hgvs_p": null,
"transcript": "NM_001329095.2",
"protein_id": "NP_001316024.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 517,
"cds_start": -4,
"cds_end": null,
"cds_length": 1554,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2580,
"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": 13,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "c.300-1605T>G",
"hgvs_p": null,
"transcript": "NM_001329097.2",
"protein_id": "NP_001316026.1",
"transcript_support_level": null,
"aa_start": null,
"aa_end": null,
"aa_length": 435,
"cds_start": -4,
"cds_end": null,
"cds_length": 1308,
"cdna_start": null,
"cdna_end": null,
"cdna_length": 2218,
"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": 12,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "c.300-9443T>G",
"hgvs_p": null,
"transcript": "ENST00000430167.1",
"protein_id": "ENSP00000406399.1",
"transcript_support_level": 2,
"aa_start": null,
"aa_end": null,
"aa_length": 399,
"cds_start": -4,
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"cds_length": 1202,
"cdna_start": null,
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"mane_select": null,
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"feature": null
},
{
"aa_ref": null,
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 8,
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"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "n.*236-1605T>G",
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"transcript": "ENST00000424136.5",
"protein_id": "ENSP00000398723.1",
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"aa_start": null,
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"cds_start": -4,
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"mane_select": null,
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"feature": null
},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 10,
"intron_rank": 3,
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"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "n.*157-1605T>G",
"hgvs_p": null,
"transcript": "ENST00000455477.5",
"protein_id": "ENSP00000399886.1",
"transcript_support_level": 5,
"aa_start": null,
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},
{
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],
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"intron_rank": 3,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
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"hgvs_c": "n.335-1605T>G",
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},
{
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"strand": false,
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"intron_variant"
],
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"gene_symbol": "GALNT14",
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"hgvs_c": "n.79-1605T>G",
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"transcript": "ENST00000481023.5",
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},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"exon_count": 3,
"intron_rank": 2,
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"gene_symbol": "GALNT14",
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"hgvs_c": "n.535-1605T>G",
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"transcript": "ENST00000490212.5",
"protein_id": null,
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},
{
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],
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"gene_symbol": "GALNT14",
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},
{
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"strand": false,
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"intron_variant"
],
"exon_rank": null,
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"exon_count": 5,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "n.529-1605T>G",
"hgvs_p": null,
"transcript": "ENST00000498206.5",
"protein_id": null,
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},
{
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"strand": false,
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],
"exon_rank": null,
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"exon_count": 17,
"intron_rank": 4,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
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"hgvs_c": "c.240-1605T>G",
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"transcript": "XM_047445827.1",
"protein_id": "XP_047301783.1",
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},
{
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],
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"gene_symbol": "GALNT14",
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"hgvs_c": "c.195-1605T>G",
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{
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],
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"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "n.304-1605T>G",
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},
{
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"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
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"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
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"hgvs_c": "n.304-1605T>G",
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"transcript": "XR_001738942.2",
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"biotype": null,
"feature": null
},
{
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"canonical": false,
"protein_coding": false,
"strand": false,
"consequences": [
"intron_variant"
],
"exon_rank": null,
"exon_rank_end": null,
"exon_count": 15,
"intron_rank": 2,
"intron_rank_end": null,
"gene_symbol": "GALNT14",
"gene_hgnc_id": 22946,
"hgvs_c": "n.304-1605T>G",
"hgvs_p": null,
"transcript": "XR_001738943.2",
"protein_id": null,
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},
{
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"strand": false,
"consequences": [
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],
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{
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],
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"splice_prediction_selected": "Benign",
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"phylop100way_prediction": "Benign",
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{
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"BP4_Strong"
],
"verdict": "Likely_benign",
"transcript": "ENST00000349752.10",
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"effects": [
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"inheritance_mode": "AR",
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}
],
"clinvar_disease": "",
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"clinvar_review_status": "",
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"phenotype_combined": null,
"pathogenicity_classification_combined": null,
"custom_annotations": null
}
],
"message": null
}