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        "NM_001145809.2:c.5788-41A>G"
      ],
      "proteinEffect": {
        "hgvs": "NP_001139281.1:n.5788-41A>G"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS677942",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000642316.2:c.5788-41A>G"
          },
          "RefSeq": {
            "hgvs": "NM_001145809.2:c.5788-41A>G"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000493594.1:n.5788-41A>G"
          },
          "RefSeq": {
            "hgvs": "NP_001139281.1:n.5788-41A>G"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "G",
          "end": 5717,
          "endIntronDirection": "-",
          "endIntronOffset": 40,
          "referenceAllele": "A",
          "start": 5717,
          "startIntronDirection": "-",
          "startIntronOffset": 41
        }
      ],
      "gene": "http://reg.genome.network/gene/GN023212",
      "geneNCBI_id": 79784,
      "geneSymbol": "MYH14",
      "hgvs": [
        "NM_024729.4:c.5665-41A>G"
      ],
      "proteinEffect": {
        "hgvs": "NP_079005.3:n.5665-41A>G"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS728666"
    }
  ],
  "type": "nucleotide"
}