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      "proteinEffect": {
        "hgvs": "NP_001304983.1:n.-149T>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS684413"
    },
    {
      "@id": "http://reg.genome.network/allele/PA2825691816",
      "coordinates": [
        {
          "allele": "C",
          "end": 385,
          "referenceAllele": "T",
          "start": 384
        }
      ],
      "gene": "http://reg.genome.network/gene/GN005173",
      "geneNCBI_id": 3265,
      "geneSymbol": "HRAS",
      "hgvs": [
        "NM_001130442.3:c.171T>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_001123914.1:p.Asp57="
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS712333"
    },
    {
      "@id": "http://reg.genome.network/allele/PA2830359629",
      "coordinates": [
        {
          "allele": "C",
          "end": 385,
          "referenceAllele": "T",
          "start": 384
        }
      ],
      "gene": "http://reg.genome.network/gene/GN005173",
      "geneNCBI_id": 3265,
      "geneSymbol": "HRAS",
      "hgvs": [
        "NM_176795.5:c.171T>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_789765.1:p.Asp57="
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS729636",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Plus Clinical",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000417302.7:c.171T>C"
          },
          "RefSeq": {
            "hgvs": "NM_176795.5:c.171T>C"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000388246.1:p.Asp57="
          },
          "RefSeq": {
            "hgvs": "NP_789765.1:p.Asp57="
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}