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      "referenceSequence": "http://reg.genome.network/refseq/RS673272",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000397746.8:c.1097T>C"
          },
          "RefSeq": {
            "hgvs": "NM_206965.2:c.1097T>C"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000380854.3:p.Met366Thr"
          },
          "RefSeq": {
            "hgvs": "NP_996848.1:p.Met366Thr"
          }
        }
      }
    },
    {
      "@id": "http://reg.genome.network/allele/PA2827044734",
      "coordinates": [
        {
          "allele": "C",
          "end": 1153,
          "referenceAllele": "T",
          "start": 1152
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003974",
      "geneNCBI_id": 10841,
      "geneSymbol": "FTCD",
      "hgvs": [
        "NM_001320412.2:c.1097T>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_001307341.1:p.Met366Thr",
        "hgvsWellDefined": "NP_001307341.1:p.Met366Thr"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS684913"
    },
    {
      "@id": "http://reg.genome.network/allele/PA2829647091",
      "coordinates": [
        {
          "allele": "C",
          "end": 1153,
          "referenceAllele": "T",
          "start": 1152
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003974",
      "geneNCBI_id": 10841,
      "geneSymbol": "FTCD",
      "hgvs": [
        "NM_006657.3:c.1097T>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_006648.1:p.Met366Thr",
        "hgvsWellDefined": "NP_006648.1:p.Met366Thr"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS696780"
    }
  ],
  "type": "nucleotide"
}