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        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000288319.12:c.19-2286G>A"
          },
          "RefSeq": {
            "hgvs": "NM_182918.4:c.19-2286G>A"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000288319.7:n.19-2286G>A"
          },
          "RefSeq": {
            "hgvs": "NP_891548.1:n.19-2286G>A"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 115,
          "endIntronDirection": "-",
          "endIntronOffset": 2285,
          "referenceAllele": "G",
          "start": 115,
          "startIntronDirection": "-",
          "startIntronOffset": 2286
        }
      ],
      "gene": "http://reg.genome.network/gene/GN003446",
      "geneNCBI_id": 2078,
      "geneSymbol": "ERG",
      "hgvs": [
        "NM_001331025.2:c.19-2286G>A"
      ],
      "proteinEffect": {
        "hgvs": "NP_001317954.1:n.19-2286G>A"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS687137"
    }
  ],
  "type": "nucleotide"
}