{
  "@context": "http://reg.genome.network/schema/allele.jsonld",
  "@id": "http://reg.genome.network/allele/CA131021",
  "communityStandardTitle": [
    "NC_012920.1:m.961T>C"
  ],
  "externalRecords": {
    "ClinVarAlleles": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/clinvar/?term=51406[alleleid]",
        "alleleId": 51406,
        "preferredName": "m.961T>C"
      }
    ],
    "ClinVarVariations": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/clinvar/variation/42236",
        "RCV": [
          "RCV000035061"
        ],
        "variationId": 42236
      }
    ],
    "MyVariantInfo_hg38": [
      {
        "@id": "http://myvariant.info/v1/variant/chrMT:g.961T>C?assembly=hg38",
        "id": "chrMT:g.961T>C"
      }
    ],
    "dbSNP": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/snp/3888511",
        "rs": 3888511
      }
    ]
  },
  "genomicAlleles": [
    {
      "chromosome": "MT",
      "coordinates": [
        {
          "allele": "C",
          "end": 961,
          "referenceAllele": "T",
          "start": 960
        }
      ],
      "hgvs": [
        "NC_012920.1:m.961T>C",
        "J01415.2:m.961T>C"
      ],
      "referenceGenome": "GRCh38",
      "referenceSequence": "http://reg.genome.network/refseq/RS000433"
    }
  ],
  "type": "nucleotide"
}