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      "hgvs": [
        "NM_001384993.1:c.1868G="
      ],
      "proteinEffect": {
        "hgvs": "NP_001371922.1:p.Trp623="
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS723363"
    },
    {
      "coordinates": [
        {
          "allele": "G",
          "end": 2055,
          "referenceAllele": "G",
          "start": 2054
        }
      ],
      "gene": "http://reg.genome.network/gene/GN011364",
      "geneNCBI_id": 6774,
      "geneSymbol": "STAT3",
      "hgvs": [
        "NM_139276.3:c.1868G="
      ],
      "proteinEffect": {
        "hgvs": "NP_644805.1:p.Trp623="
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS729226",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000264657.10:c.1868G="
          },
          "RefSeq": {
            "hgvs": "NM_139276.3:c.1868G="
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000264657.4:p.Trp623="
          },
          "RefSeq": {
            "hgvs": "NP_644805.1:p.Trp623="
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}