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        "hgvs": "XP_016857517.1:p.Thr3176Ile",
        "hgvsWellDefined": "XP_016857517.1:p.Thr3176Ile"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS558067"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 9812,
          "referenceAllele": "C",
          "start": 9811
        }
      ],
      "gene": "http://reg.genome.network/gene/GN010484",
      "geneNCBI_id": 6262,
      "geneSymbol": "RYR2",
      "hgvs": [
        "XR_949152.2:n.9812C>T"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS615229"
    },
    {
      "@id": "http://reg.genome.network/allele/PA306899",
      "coordinates": [
        {
          "allele": "T",
          "end": 9856,
          "referenceAllele": "C",
          "start": 9855
        }
      ],
      "gene": "http://reg.genome.network/gene/GN010484",
      "geneNCBI_id": 6262,
      "geneSymbol": "RYR2",
      "hgvs": [
        "NM_001035.3:c.9518C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_001026.2:p.Thr3173Ile",
        "hgvsWellDefined": "NP_001026.2:p.Thr3173Ile"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS663078",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000366574.7:c.9518C>T"
          },
          "RefSeq": {
            "hgvs": "NM_001035.3:c.9518C>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000355533.2:p.Thr3173Ile"
          },
          "RefSeq": {
            "hgvs": "NP_001026.2:p.Thr3173Ile"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}