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      "proteinEffect": {
        "hgvs": "XP_024308866.1:p.Tyr1629="
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS586485"
    },
    {
      "coordinates": [
        {
          "allele": "A",
          "end": 5111,
          "referenceAllele": "A",
          "start": 5110
        }
      ],
      "gene": "http://reg.genome.network/gene/GN012403",
      "geneNCBI_id": 7273,
      "geneSymbol": "TTN",
      "hgvs": [
        "XM_024453099.1:c.4886A="
      ],
      "proteinEffect": {
        "hgvs": "XP_024308867.1:p.Tyr1629="
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      "referenceSequence": "http://reg.genome.network/refseq/RS586486"
    },
    {
      "@id": "http://reg.genome.network/allele/PA3067381503",
      "coordinates": [
        {
          "allele": "A",
          "end": 5108,
          "referenceAllele": "A",
          "start": 5107
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      "gene": "http://reg.genome.network/gene/GN012403",
      "geneNCBI_id": 7273,
      "geneSymbol": "TTN",
      "hgvs": [
        "NM_133379.5:c.4883A="
      ],
      "proteinEffect": {
        "hgvs": "NP_596870.2:p.Tyr1628="
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS699650",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Plus Clinical",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000360870.10:c.4883A="
          },
          "RefSeq": {
            "hgvs": "NM_133379.5:c.4883A="
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        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000354117.4:p.Tyr1628="
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        }
      }
    }
  ],
  "type": "nucleotide"
}