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        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000261866.12:c.5011C>T"
          },
          "RefSeq": {
            "hgvs": "NM_025137.4:c.5011C>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000261866.7:p.His1671Tyr"
          },
          "RefSeq": {
            "hgvs": "NP_079413.3:p.His1671Tyr"
          }
        }
      }
    },
    {
      "@id": "http://reg.genome.network/allele/PA2825948089",
      "coordinates": [
        {
          "allele": "T",
          "end": 5026,
          "referenceAllele": "C",
          "start": 5025
        }
      ],
      "gene": "http://reg.genome.network/gene/GN011226",
      "geneNCBI_id": 80208,
      "geneSymbol": "SPG11",
      "hgvs": [
        "NM_001160227.2:c.5011C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_001153699.1:p.His1671Tyr",
        "hgvsWellDefined": "NP_001153699.1:p.His1671Tyr"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS678139"
    }
  ],
  "type": "nucleotide"
}