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        "NM_001379050.1:c.*1350A>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_001365979.1:n.*1350A>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS721901"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 3470,
          "referenceAllele": "A",
          "start": 3469
        }
      ],
      "gene": "http://reg.genome.network/gene/GN016380",
      "geneNCBI_id": 22954,
      "geneSymbol": "TRIM32",
      "hgvs": [
        "NM_012210.4:c.*1350A>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_036342.2:n.*1350A>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS727851",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000450136.2:c.*1350A>C"
          },
          "RefSeq": {
            "hgvs": "NM_012210.4:c.*1350A>C"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000408292.1:n.*1350A>C"
          },
          "RefSeq": {
            "hgvs": "NP_036342.2:n.*1350A>C"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}