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      "proteinEffect": {
        "hgvs": "XP_024303186.1:n.170+14276G>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS581001"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 393,
          "endIntronDirection": "+",
          "endIntronOffset": 14276,
          "referenceAllele": "G",
          "start": 393,
          "startIntronDirection": "+",
          "startIntronOffset": 14275
        }
      ],
      "gene": "http://reg.genome.network/gene/GN017294",
      "geneNCBI_id": 153090,
      "geneSymbol": "DAB2IP",
      "hgvs": [
        "NM_032552.4:c.278+14276G>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_115941.2:n.278+14276G>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS728854"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 504,
          "endIntronDirection": "+",
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          "referenceAllele": "G",
          "start": 504,
          "startIntronDirection": "+",
          "startIntronOffset": 14275
        }
      ],
      "gene": "http://reg.genome.network/gene/GN017294",
      "geneNCBI_id": 153090,
      "geneSymbol": "DAB2IP",
      "hgvs": [
        "NM_001395010.1:c.362+14276G>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_001381939.1:n.362+14276G>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS782614",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000408936.8:c.362+14276G>T"
          },
          "RefSeq": {
            "hgvs": "NM_001395010.1:c.362+14276G>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000386183.3:n.362+14276G>T"
          },
          "RefSeq": {
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          }
        }
      }
    }
  ],
  "type": "nucleotide"
}