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          "Ensembl": {
            "hgvs": "ENST00000311189.8:c.35G>T"
          },
          "RefSeq": {
            "hgvs": "NM_005343.4:c.35G>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000309845.7:p.Gly12Val"
          },
          "RefSeq": {
            "hgvs": "NP_005334.1:p.Gly12Val"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 249,
          "referenceAllele": "G",
          "start": 248
        }
      ],
      "gene": "http://reg.genome.network/gene/GN005173",
      "geneNCBI_id": 3265,
      "geneSymbol": "HRAS",
      "hgvs": [
        "NM_001318054.2:c.-285G>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_001304983.1:n.-285G>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS684413"
    },
    {
      "@id": "http://reg.genome.network/allele/PA103611",
      "coordinates": [
        {
          "allele": "T",
          "end": 249,
          "referenceAllele": "G",
          "start": 248
        }
      ],
      "gene": "http://reg.genome.network/gene/GN005173",
      "geneNCBI_id": 3265,
      "geneSymbol": "HRAS",
      "hgvs": [
        "NM_001130442.3:c.35G>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_001123914.1:p.Gly12Val",
        "hgvsWellDefined": "NP_001123914.1:p.Gly12Val"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS712333"
    },
    {
      "@id": "http://reg.genome.network/allele/PA916071670",
      "coordinates": [
        {
          "allele": "T",
          "end": 249,
          "referenceAllele": "G",
          "start": 248
        }
      ],
      "gene": "http://reg.genome.network/gene/GN005173",
      "geneNCBI_id": 3265,
      "geneSymbol": "HRAS",
      "hgvs": [
        "NM_176795.5:c.35G>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_789765.1:p.Gly12Val",
        "hgvsWellDefined": "NP_789765.1:p.Gly12Val"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS729636",
      "MANE": {
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        "maneStatus": "MANE Plus Clinical",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000417302.7:c.35G>T"
          },
          "RefSeq": {
            "hgvs": "NM_176795.5:c.35G>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000388246.1:p.Gly12Val"
          },
          "RefSeq": {
            "hgvs": "NP_789765.1:p.Gly12Val"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}