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          "referenceAllele": "G",
          "start": 751,
          "startIntronDirection": "+",
          "startIntronOffset": 2902
        }
      ],
      "gene": "http://reg.genome.network/gene/GN019022",
      "geneNCBI_id": 259217,
      "geneSymbol": "HSPA12A",
      "hgvs": [
        "NM_001330164.2:c.597+2903G>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_001317093.1:n.597+2903G>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS686786"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 643,
          "endIntronDirection": "+",
          "endIntronOffset": 2903,
          "referenceAllele": "G",
          "start": 643,
          "startIntronDirection": "+",
          "startIntronOffset": 2902
        }
      ],
      "gene": "http://reg.genome.network/gene/GN019022",
      "geneNCBI_id": 259217,
      "geneSymbol": "HSPA12A",
      "hgvs": [
        "NM_025015.3:c.546+2903G>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_079291.2:n.546+2903G>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS698804",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000369209.8:c.546+2903G>C"
          },
          "RefSeq": {
            "hgvs": "NM_025015.3:c.546+2903G>C"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000358211.3:n.546+2903G>C"
          },
          "RefSeq": {
            "hgvs": "NP_079291.2:n.546+2903G>C"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}