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        "NM_003459.5:c.96-1299C>G"
      ],
      "proteinEffect": {
        "hgvs": "NP_003450.2:n.96-1299C>G"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS695838",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000233535.9:c.96-1299C>G"
          },
          "RefSeq": {
            "hgvs": "NM_003459.5:c.96-1299C>G"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000233535.4:n.96-1299C>G"
          },
          "RefSeq": {
            "hgvs": "NP_003450.2:n.96-1299C>G"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "G",
          "end": 363,
          "endIntronDirection": "-",
          "endIntronOffset": 1298,
          "referenceAllele": "C",
          "start": 363,
          "startIntronDirection": "-",
          "startIntronOffset": 1299
        }
      ],
      "gene": "http://reg.genome.network/gene/GN011014",
      "geneNCBI_id": 7781,
      "geneSymbol": "SLC30A3",
      "hgvs": [
        "NM_001318950.2:c.57-1299C>G"
      ],
      "proteinEffect": {
        "hgvs": "NP_001305879.1:n.57-1299C>G"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS717637"
    }
  ],
  "type": "nucleotide"
}