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      "@id": "http://reg.genome.network/allele/PA2825987223",
      "coordinates": [
        {
          "allele": "A",
          "end": 25756,
          "referenceAllele": "G",
          "start": 25755
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      ],
      "gene": "http://reg.genome.network/gene/GN007720",
      "geneNCBI_id": 4703,
      "geneSymbol": "NEB",
      "hgvs": [
        "NM_001164507.2:c.25564G>A"
      ],
      "proteinEffect": {
        "hgvs": "NP_001157979.2:p.Val8522Ile",
        "hgvsWellDefined": "NP_001157979.2:p.Val8522Ile"
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      "referenceSequence": "http://reg.genome.network/refseq/RS713104",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Plus Clinical",
        "nucleotide": {
          "Ensembl": {
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          "RefSeq": {
            "hgvs": "NM_001164507.2:c.25564G>A"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000416578.2:p.Val8522Ile"
          },
          "RefSeq": {
            "hgvs": "NP_001157979.2:p.Val8522Ile"
          }
        }
      }
    },
    {
      "@id": "http://reg.genome.network/allele/PA2825994178",
      "coordinates": [
        {
          "allele": "A",
          "end": 25756,
          "referenceAllele": "G",
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        }
      ],
      "gene": "http://reg.genome.network/gene/GN007720",
      "geneNCBI_id": 4703,
      "geneSymbol": "NEB",
      "hgvs": [
        "NM_001164508.2:c.25564G>A"
      ],
      "proteinEffect": {
        "hgvs": "NP_001157980.2:p.Val8522Ile",
        "hgvsWellDefined": "NP_001157980.2:p.Val8522Ile"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS713105",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
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        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000380505.3:p.Val8522Ile"
          },
          "RefSeq": {
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          }
        }
      }
    }
  ],
  "type": "nucleotide"
}