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        "NM_014363.6:c.9909T>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_055178.3:p.Pro3303="
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS668309",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000382292.9:c.9909T>C"
          },
          "RefSeq": {
            "hgvs": "NM_014363.6:c.9909T>C"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000371729.3:p.Pro3303="
          },
          "RefSeq": {
            "hgvs": "NP_055178.3:p.Pro3303="
          }
        }
      }
    },
    {
      "@id": "http://reg.genome.network/allele/PA2826578107",
      "coordinates": [
        {
          "allele": "C",
          "end": 9958,
          "referenceAllele": "T",
          "start": 9957
        }
      ],
      "gene": "http://reg.genome.network/gene/GN010519",
      "geneNCBI_id": 26278,
      "geneSymbol": "SACS",
      "hgvs": [
        "NM_001278055.2:c.9468T>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_001264984.1:p.Pro3156="
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS681389"
    }
  ],
  "type": "nucleotide"
}