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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: 19-54143436-C-A (hg38)

Bash / cURL Example

bash
curl "https://api.genebe.net/cloud/api-public/v1/variant?chr=19&pos=54143436&ref=C&alt=A&genome=hg38&allGenes=true"

API Response

json
{
  "variants": [
    {
      "chr": "19",
      "pos": 54143436,
      "ref": "C",
      "alt": "A",
      "effect": "splice_region_variant,intron_variant",
      "transcript": "NM_001440653.1",
      "consequences": [
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "NM_014516.4",
          "protein_id": "NP_055331.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 753,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2262,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "ENST00000221232.11",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_014516.4"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": true,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "ENST00000221232.11",
          "protein_id": "ENSP00000221232.5",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 753,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2262,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": "NM_014516.4",
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000221232.11"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 17,
          "intron_rank": 2,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "ENST00000358389.7",
          "protein_id": "ENSP00000351159.4",
          "transcript_support_level": 1,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 753,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2262,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "ENST00000358389.7"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "NM_001440653.1",
          "protein_id": "NP_001427582.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 771,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2316,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440653.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "NM_001440654.1",
          "protein_id": "NP_001427583.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 770,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2313,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440654.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "NM_001440655.1",
          "protein_id": "NP_001427584.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 757,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2274,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440655.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "NM_001440656.1",
          "protein_id": "NP_001427585.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 756,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2271,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440656.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "NM_001440661.1",
          "protein_id": "NP_001427590.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 754,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2265,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440661.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "NM_001440662.1",
          "protein_id": "NP_001427591.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 754,
          "cds_start": null,
          "cds_end": null,
          "cds_length": 2265,
          "cdna_start": null,
          "cdna_end": null,
          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
          "feature": "NM_001440662.1"
        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "ENST00000896564.1",
          "protein_id": "ENSP00000566623.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 754,
          "cds_start": null,
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          "cds_length": 2265,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
          "mane_plus": null,
          "biotype": "protein_coding",
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        },
        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "ENST00000933501.1",
          "protein_id": "ENSP00000603560.1",
          "transcript_support_level": null,
          "aa_start": null,
          "aa_end": null,
          "aa_length": 754,
          "cds_start": null,
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          "cds_length": 2265,
          "cdna_start": null,
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          "cdna_length": null,
          "mane_select": null,
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          "biotype": "protein_coding",
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        {
          "aa_ref": null,
          "aa_alt": null,
          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
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            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "ENST00000933506.1",
          "protein_id": "ENSP00000603565.1",
          "transcript_support_level": null,
          "aa_start": null,
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          "aa_length": 754,
          "cds_start": null,
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          "cdna_start": null,
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        },
        {
          "aa_ref": null,
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
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          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 4,
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          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
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          "transcript": "ENST00000896565.1",
          "protein_id": "ENSP00000566624.1",
          "transcript_support_level": null,
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          "cds_start": null,
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          "mane_select": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000896565.1"
        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
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          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "ENST00000933502.1",
          "protein_id": "ENSP00000603561.1",
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        {
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            "intron_variant"
          ],
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          "intron_rank": 3,
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          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "ENST00000933503.1",
          "protein_id": "ENSP00000603562.1",
          "transcript_support_level": null,
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          "cdna_start": null,
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          "biotype": "protein_coding",
          "feature": "ENST00000933503.1"
        },
        {
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          "canonical": false,
          "protein_coding": true,
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          "consequences": [
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          ],
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          "exon_count": 19,
          "intron_rank": 4,
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          "gene_symbol": "CNOT3",
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          "hgvs_c": "c.94-6C>A",
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          "transcript": "ENST00000933504.1",
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        },
        {
          "aa_ref": null,
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          "canonical": false,
          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 19,
          "intron_rank": 4,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
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        {
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          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
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          "transcript": "ENST00000933509.1",
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        {
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          "strand": true,
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          ],
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          "intron_rank": 3,
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          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
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          "transcript": "ENST00000933512.1",
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          "biotype": "protein_coding",
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        },
        {
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          "protein_coding": true,
          "strand": true,
          "consequences": [
            "splice_region_variant",
            "intron_variant"
          ],
          "exon_rank": null,
          "exon_rank_end": null,
          "exon_count": 18,
          "intron_rank": 3,
          "intron_rank_end": null,
          "gene_symbol": "CNOT3",
          "gene_hgnc_id": 7879,
          "hgvs_c": "c.94-6C>A",
          "hgvs_p": null,
          "transcript": "ENST00000933508.1",
          "protein_id": "ENSP00000603567.1",
          "transcript_support_level": null,
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      "acmg_criteria": "PM2,BP4_Moderate",
      "acmg_by_gene": [
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            "BP4_Moderate"
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          "verdict": "Uncertain_significance",
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      "clinvar_classification": "Uncertain significance",
      "clinvar_review_status": "criteria provided, single submitter",
      "clinvar_submissions_summary": "US:1",
      "phenotype_combined": "Intellectual developmental disorder with speech delay, autism, and dysmorphic facies",
      "pathogenicity_classification_combined": "Uncertain significance",
      "custom_annotations": null
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  "message": null
}