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        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000263360.11:c.1199+10T>C"
          },
          "RefSeq": {
            "hgvs": "NM_003797.5:c.1199+10T>C"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000263360.6:n.1199+10T>C"
          },
          "RefSeq": {
            "hgvs": "NP_003788.2:n.1199+10T>C"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 1751,
          "endIntronDirection": "+",
          "endIntronOffset": 10,
          "referenceAllele": "T",
          "start": 1751,
          "startIntronDirection": "+",
          "startIntronOffset": 9
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003188",
      "geneNCBI_id": 8726,
      "geneSymbol": "EED",
      "hgvs": [
        "NM_001308007.2:c.1274+10T>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_001294936.1:n.1274+10T>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS717200"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 1436,
          "endIntronDirection": "+",
          "endIntronOffset": 10,
          "referenceAllele": "T",
          "start": 1436,
          "startIntronDirection": "+",
          "startIntronOffset": 9
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003188",
      "geneNCBI_id": 8726,
      "geneSymbol": "EED",
      "hgvs": [
        "NM_001330334.2:c.959+10T>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_001317263.1:n.959+10T>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS718653"
    }
  ],
  "type": "nucleotide"
}