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      "geneNCBI_id": 80332,
      "geneSymbol": "ADAM33",
      "hgvs": [
        "NM_025220.5:c.2320C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_079496.1:p.Pro774Ser",
        "hgvsWellDefined": "NP_079496.1:p.Pro774Ser"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS698839",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000356518.7:c.2320C>T"
          },
          "RefSeq": {
            "hgvs": "NM_025220.5:c.2320C>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000348912.3:p.Pro774Ser"
          },
          "RefSeq": {
            "hgvs": "NP_079496.1:p.Pro774Ser"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 2248,
          "referenceAllele": "C",
          "start": 2247
        }
      ],
      "gene": "http://reg.genome.network/gene/GN015478",
      "geneNCBI_id": 80332,
      "geneSymbol": "ADAM33",
      "hgvs": [
        "NM_153202.4:c.2242C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_694882.1:p.Pro748Ser",
        "hgvsWellDefined": "NP_694882.1:p.Pro748Ser"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS700319"
    }
  ],
  "type": "nucleotide"
}