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      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000337836.10:c.293A>C"
          },
          "RefSeq": {
            "hgvs": "NM_000065.5:c.293A>C"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000338861.5:p.Glu98Ala"
          },
          "RefSeq": {
            "hgvs": "NP_000056.2:p.Glu98Ala"
          }
        }
      }
    },
    {
      "@id": "http://reg.genome.network/allele/PA915976881",
      "coordinates": [
        {
          "allele": "C",
          "end": 589,
          "referenceAllele": "A",
          "start": 588
        }
      ],
      "gene": "http://reg.genome.network/gene/GN001339",
      "geneNCBI_id": 729,
      "geneSymbol": "C6",
      "hgvs": [
        "NM_001115131.4:c.293A>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_001108603.2:p.Glu98Ala",
        "hgvsWellDefined": "NP_001108603.2:p.Glu98Ala"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS712135"
    }
  ],
  "type": "nucleotide"
}