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        "XM_017023173.1:c.808C>T"
      ],
      "proteinEffect": {
        "hgvs": "XP_016878662.1:p.Gln270Ter"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS573977"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 1222,
          "referenceAllele": "C",
          "start": 1221
        }
      ],
      "gene": "http://reg.genome.network/gene/GN004585",
      "geneNCBI_id": 2903,
      "geneSymbol": "GRIN2A",
      "hgvs": [
        "NM_001134407.3:c.652C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_001127879.1:p.Gln218Ter"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS663623",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000330684.4:c.652C>T"
          },
          "RefSeq": {
            "hgvs": "NM_001134407.3:c.652C>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000332549.3:p.Gln218Ter"
          },
          "RefSeq": {
            "hgvs": "NP_001127879.1:p.Gln218Ter"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 1116,
          "referenceAllele": "C",
          "start": 1115
        }
      ],
      "gene": "http://reg.genome.network/gene/GN004585",
      "geneNCBI_id": 2903,
      "geneSymbol": "GRIN2A",
      "hgvs": [
        "NM_000833.5:c.652C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_000824.1:p.Gln218Ter"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS674962"
    }
  ],
  "type": "nucleotide"
}