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        "hgvs": "NP_001263274.1:p.Phe120Val",
        "hgvsWellDefined": "NP_001263274.1:p.Phe120Val"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS681301",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000656932.1:c.358T>G"
          },
          "RefSeq": {
            "hgvs": "NM_001276345.2:c.358T>G"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000499593.1:p.Phe120Val"
          },
          "RefSeq": {
            "hgvs": "NP_001263274.1:p.Phe120Val"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "G",
          "end": 363,
          "endIntronDirection": "+",
          "endIntronOffset": 366,
          "referenceAllele": "T",
          "start": 363,
          "startIntronDirection": "+",
          "startIntronOffset": 365
        }
      ],
      "gene": "http://reg.genome.network/gene/GN011949",
      "geneNCBI_id": 7139,
      "geneSymbol": "TNNT2",
      "hgvs": [
        "NM_001276346.2:c.291+366T>G"
      ],
      "proteinEffect": {
        "hgvs": "NP_001263275.1:n.291+366T>G"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS681302"
    },
    {
      "@id": "http://reg.genome.network/allele/PA2826555246",
      "coordinates": [
        {
          "allele": "G",
          "end": 533,
          "referenceAllele": "T",
          "start": 532
        }
      ],
      "gene": "http://reg.genome.network/gene/GN011949",
      "geneNCBI_id": 7139,
      "geneSymbol": "TNNT2",
      "hgvs": [
        "NM_001276347.2:c.328T>G"
      ],
      "proteinEffect": {
        "hgvs": "NP_001263276.1:p.Phe110Val",
        "hgvsWellDefined": "NP_001263276.1:p.Phe110Val"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS681303"
    }
  ],
  "type": "nucleotide"
}