{
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  "@id": "http://reg.genome.network/allele/CA337097609",
  "communityStandardTitle": [
    "NC_012920.1:m.7389T>C"
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  "externalRecords": {
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      {
        "@id": "http://www.ncbi.nlm.nih.gov/clinvar/?term=681277[alleleid]",
        "alleleId": 681277,
        "preferredName": "NC_012920.1(MT-CO1):m.7389T>C"
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    "ClinVarVariations": [
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        "@id": "http://www.ncbi.nlm.nih.gov/clinvar/variation/692741",
        "RCV": [
          "RCV000854066"
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      {
        "@id": "http://myvariant.info/v1/variant/chrMT:g.7389T>C?assembly=hg38",
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  "genomicAlleles": [
    {
      "chromosome": "MT",
      "coordinates": [
        {
          "allele": "C",
          "end": 7389,
          "referenceAllele": "T",
          "start": 7388
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      "hgvs": [
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      "referenceGenome": "GRCh38",
      "referenceSequence": "http://reg.genome.network/refseq/RS000433"
    }
  ],
  "transcriptAlleles": [
    {
      "coordinates": [
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          "end": 1486,
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        }
      ],
      "gene": "http://reg.genome.network/gene/GN007419",
      "geneNCBI_id": 4512,
      "geneSymbol": "MT-CO1",
      "hgvs": [
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      ],
      "proteinEffect": {
        "hgvs": "ENSP00000354499.2:p.Tyr496His",
        "hgvsWellDefined": "ENSP00000354499.2:p.Tyr496His"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS265570"
    }
  ],
  "type": "nucleotide"
}