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        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000393545.9:c.923G>A"
          },
          "RefSeq": {
            "hgvs": "NM_018418.5:c.923G>A"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000377176.4:p.Cys308Tyr"
          },
          "RefSeq": {
            "hgvs": "NP_060888.2:p.Cys308Tyr"
          }
        }
      }
    },
    {
      "@id": "http://reg.genome.network/allele/PA2825363637",
      "coordinates": [
        {
          "allele": "A",
          "end": 989,
          "referenceAllele": "G",
          "start": 988
        }
      ],
      "gene": "http://reg.genome.network/gene/GN020423",
      "geneNCBI_id": 55812,
      "geneSymbol": "SPATA7",
      "hgvs": [
        "NM_001040428.4:c.827G>A"
      ],
      "proteinEffect": {
        "hgvs": "NP_001035518.1:p.Cys276Tyr",
        "hgvsWellDefined": "NP_001035518.1:p.Cys276Tyr"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS711647"
    }
  ],
  "type": "nucleotide"
}