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        "hgvs": "NP_001358999.1:n.-196+1603C>G"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS693128"
    },
    {
      "coordinates": [
        {
          "allele": "G",
          "end": 260,
          "endIntronDirection": "-",
          "endIntronOffset": 1689,
          "referenceAllele": "C",
          "start": 260,
          "startIntronDirection": "-",
          "startIntronOffset": 1690
        }
      ],
      "gene": "http://reg.genome.network/gene/GN028952",
      "geneNCBI_id": 23310,
      "geneSymbol": "NCAPD3",
      "hgvs": [
        "NM_015261.3:c.220-1690C>G"
      ],
      "proteinEffect": {
        "hgvs": "NP_056076.1:n.220-1690C>G"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS697487",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000534548.7:c.220-1690C>G"
          },
          "RefSeq": {
            "hgvs": "NM_015261.3:c.220-1690C>G"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000433681.3:n.220-1690C>G"
          },
          "RefSeq": {
            "hgvs": "NP_056076.1:n.220-1690C>G"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}