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      "proteinEffect": {
        "hgvs": "NP_000422.1:p.Ala148Thr",
        "hgvsWellDefined": "NP_000422.1:p.Ala148Thr"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS662441",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000228510.8:c.442G>A"
          },
          "RefSeq": {
            "hgvs": "NM_000431.4:c.442G>A"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000228510.3:p.Ala148Thr"
          },
          "RefSeq": {
            "hgvs": "NP_000422.1:p.Ala148Thr"
          }
        }
      }
    },
    {
      "@id": "http://reg.genome.network/allele/PA645481406",
      "coordinates": [
        {
          "allele": "A",
          "end": 527,
          "referenceAllele": "G",
          "start": 526
        }
      ],
      "gene": "http://reg.genome.network/gene/GN007530",
      "geneNCBI_id": 4598,
      "geneSymbol": "MVK",
      "hgvs": [
        "NM_001114185.3:c.442G>A"
      ],
      "proteinEffect": {
        "hgvs": "NP_001107657.1:p.Ala148Thr",
        "hgvsWellDefined": "NP_001107657.1:p.Ala148Thr"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS676743"
    },
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 465,
          "endIntronDirection": "+",
          "endIntronOffset": 1519,
          "referenceAllele": "G",
          "start": 465,
          "startIntronDirection": "+",
          "startIntronOffset": 1518
        }
      ],
      "gene": "http://reg.genome.network/gene/GN007530",
      "geneNCBI_id": 4598,
      "geneSymbol": "MVK",
      "hgvs": [
        "NM_001301182.2:c.371+1519G>A"
      ],
      "proteinEffect": {
        "hgvs": "NP_001288111.1:n.371+1519G>A"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS683373"
    }
  ],
  "type": "nucleotide"
}