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        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000358901.11:c.572G>A"
          },
          "RefSeq": {
            "hgvs": "NM_007126.5:c.572G>A"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000351777.6:p.Arg191Gln"
          },
          "RefSeq": {
            "hgvs": "NP_009057.1:p.Arg191Gln"
          }
        }
      }
    },
    {
      "@id": "http://reg.genome.network/allele/PA2828037034",
      "coordinates": [
        {
          "allele": "A",
          "end": 904,
          "referenceAllele": "G",
          "start": 903
        }
      ],
      "gene": "http://reg.genome.network/gene/GN012666",
      "geneNCBI_id": 7415,
      "geneSymbol": "VCP",
      "hgvs": [
        "NM_001354927.2:c.437G>A"
      ],
      "proteinEffect": {
        "hgvs": "NP_001341856.1:p.Arg146Gln",
        "hgvsWellDefined": "NP_001341856.1:p.Arg146Gln"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS720585"
    },
    {
      "@id": "http://reg.genome.network/allele/PA2828037520",
      "coordinates": [
        {
          "allele": "A",
          "end": 1424,
          "referenceAllele": "G",
          "start": 1423
        }
      ],
      "gene": "http://reg.genome.network/gene/GN012666",
      "geneNCBI_id": 7415,
      "geneSymbol": "VCP",
      "hgvs": [
        "NM_001354928.2:c.437G>A"
      ],
      "proteinEffect": {
        "hgvs": "NP_001341857.1:p.Arg146Gln",
        "hgvsWellDefined": "NP_001341857.1:p.Arg146Gln"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS720586"
    }
  ],
  "type": "nucleotide"
}