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        "hgvs": "XP_011510268.2:n.3049-3882A>C"
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      "referenceSequence": "http://reg.genome.network/refseq/RS542363"
    },
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          "allele": "G",
          "end": 2941,
          "endIntronDirection": "+",
          "endIntronOffset": 287,
          "referenceAllele": "T",
          "start": 2941,
          "startIntronDirection": "+",
          "startIntronOffset": 286
        }
      ],
      "gene": "http://reg.genome.network/gene/GN017063",
      "geneNCBI_id": 22930,
      "geneSymbol": "RAB3GAP1",
      "hgvs": [
        "XR_001738674.2:n.2941+287T>G"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS589149"
    },
    {
      "coordinates": [
        {
          "allele": "G",
          "end": 3238,
          "referenceAllele": "T",
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      "gene": "http://reg.genome.network/gene/GN017063",
      "geneNCBI_id": 22930,
      "geneSymbol": "RAB3GAP1",
      "hgvs": [
        "NM_001172435.2:c.*255T>G"
      ],
      "proteinEffect": {
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      },
      "referenceSequence": "http://reg.genome.network/refseq/RS678754"
    },
    {
      "coordinates": [
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      ],
      "gene": "http://reg.genome.network/gene/GN017063",
      "geneNCBI_id": 22930,
      "geneSymbol": "RAB3GAP1",
      "hgvs": [
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      ],
      "proteinEffect": {
        "hgvs": "NP_036365.1:n.*255T>G"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS697025",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000264158.13:c.*255T>G"
          },
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            "hgvs": "NM_012233.3:c.*255T>G"
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        },
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          "Ensembl": {
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        }
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    }
  ],
  "type": "nucleotide"
}