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        "hgvs": "XP_016857517.1:n.11178+4081C>A"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS558067"
    },
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 11483,
          "endIntronDirection": "+",
          "endIntronOffset": 5355,
          "referenceAllele": "C",
          "start": 11483,
          "startIntronDirection": "+",
          "startIntronOffset": 5354
        }
      ],
      "gene": "http://reg.genome.network/gene/GN010484",
      "geneNCBI_id": 6262,
      "geneSymbol": "RYR2",
      "hgvs": [
        "NM_001035.3:c.11145+5355C>A"
      ],
      "proteinEffect": {
        "hgvs": "NP_001026.2:n.11145+5355C>A"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS663078",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000366574.7:c.11145+5355C>A"
          },
          "RefSeq": {
            "hgvs": "NM_001035.3:c.11145+5355C>A"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000355533.2:n.11145+5355C>A"
          },
          "RefSeq": {
            "hgvs": "NP_001026.2:n.11145+5355C>A"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}