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      "proteinEffect": {
        "hgvs": "NP_002038.2:p.Met292Arg",
        "hgvsWellDefined": "NP_002038.2:p.Met292Arg"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS027373"
    },
    {
      "coordinates": [
        {
          "allele": "G",
          "end": 763,
          "referenceAllele": "T",
          "start": 762
        }
      ],
      "gene": "http://reg.genome.network/gene/GN004162",
      "geneNCBI_id": 2617,
      "geneSymbol": "GARS1",
      "hgvs": [
        "XM_006715686.1:c.506T>G"
      ],
      "proteinEffect": {
        "hgvs": "XP_006715749.1:p.Met169Arg",
        "hgvsWellDefined": "XP_006715749.1:p.Met169Arg"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS071297"
    },
    {
      "coordinates": [
        {
          "allele": "G",
          "end": 1064,
          "referenceAllele": "T",
          "start": 1063
        }
      ],
      "gene": "http://reg.genome.network/gene/GN004162",
      "geneNCBI_id": 2617,
      "geneSymbol": "GARS1",
      "hgvs": [
        "XM_006715686.2:c.506T>G"
      ],
      "proteinEffect": {
        "hgvs": "XP_006715749.1:p.Met169Arg",
        "hgvsWellDefined": "XP_006715749.1:p.Met169Arg"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS539002"
    },
    {
      "@id": "http://reg.genome.network/allele/PA658660183",
      "coordinates": [
        {
          "allele": "G",
          "end": 919,
          "referenceAllele": "T",
          "start": 918
        }
      ],
      "gene": "http://reg.genome.network/gene/GN004162",
      "geneNCBI_id": 2617,
      "geneSymbol": "GARS1",
      "hgvs": [
        "NM_002047.4:c.875T>G"
      ],
      "proteinEffect": {
        "hgvs": "NP_002038.2:p.Met292Arg",
        "hgvsWellDefined": "NP_002038.2:p.Met292Arg"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS665317",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000389266.8:c.875T>G"
          },
          "RefSeq": {
            "hgvs": "NM_002047.4:c.875T>G"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000373918.3:p.Met292Arg"
          },
          "RefSeq": {
            "hgvs": "NP_002038.2:p.Met292Arg"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}