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        "hgvs": "XP_016869871.1:n.239+15A>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS567393"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 690,
          "endIntronDirection": "+",
          "endIntronOffset": 15,
          "referenceAllele": "A",
          "start": 690,
          "startIntronDirection": "+",
          "startIntronOffset": 14
        }
      ],
      "gene": "http://reg.genome.network/gene/GN000029",
      "geneNCBI_id": 19,
      "geneSymbol": "ABCA1",
      "hgvs": [
        "XR_001746223.1:n.690+15A>T"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS594577"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 615,
          "endIntronDirection": "+",
          "endIntronOffset": 15,
          "referenceAllele": "A",
          "start": 615,
          "startIntronDirection": "+",
          "startIntronOffset": 14
        }
      ],
      "gene": "http://reg.genome.network/gene/GN000029",
      "geneNCBI_id": 19,
      "geneSymbol": "ABCA1",
      "hgvs": [
        "NM_005502.4:c.302+15A>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_005493.2:n.302+15A>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS666998",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000374736.8:c.302+15A>T"
          },
          "RefSeq": {
            "hgvs": "NM_005502.4:c.302+15A>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000363868.3:n.302+15A>T"
          },
          "RefSeq": {
            "hgvs": "NP_005493.2:n.302+15A>T"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}