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          "Ensembl": {
            "hgvs": "ENST00000636930.2:c.1337C>T"
          },
          "RefSeq": {
            "hgvs": "NM_001374828.1:c.1337C>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000490491.2:p.Ala446Val"
          },
          "RefSeq": {
            "hgvs": "NP_001361757.1:p.Ala446Val"
          }
        }
      }
    },
    {
      "@id": "http://reg.genome.network/allele/PA2573092759",
      "coordinates": [
        {
          "allele": "T",
          "end": 1640,
          "referenceAllele": "C",
          "start": 1639
        }
      ],
      "gene": "http://reg.genome.network/gene/GN018040",
      "geneNCBI_id": 57492,
      "geneSymbol": "ARID1B",
      "hgvs": [
        "NM_017519.3:c.1337C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_059989.3:p.Ala446Val",
        "hgvsWellDefined": "NP_059989.3:p.Ala446Val"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS697814"
    }
  ],
  "type": "nucleotide"
}