{
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  "communityStandardTitle": [
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          "RCV000952685"
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      {
        "@id": "http://myvariant.info/v1/variant/chr10:g.118969015_118969016insT?assembly=hg19",
        "id": "chr10:g.118969015_118969016insT"
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        "id": "chr10:g.117209505dupT"
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        "variant": "10:117209504 C / CT"
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        "@id": "http://gnomad.broadinstitute.org/variant/10-117209504-C-CT?dataset=gnomad_r4",
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      "referenceSequence": "http://reg.genome.network/refseq/RS000058"
    },
    {
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          "referenceAllele": "",
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    },
    {
      "chromosome": "10",
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          "referenceAllele": "",
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    {
      "coordinates": [
        {
          "allele": "T",
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          "referenceAllele": "",
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      "hgvs": [
        "NG_028085.1:g.17017dup"
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      "referenceSequence": "http://reg.genome.network/refseq/RS004065"
    }
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        {
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          "referenceAllele": "",
          "start": 361
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      ],
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          }
        },
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            "hgvs": "ENSP00000334650.1:p.Tyr121LeufsTer?"
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            "hgvs": "NP_862823.1:p.Tyr121LeufsTer?"
          }
        }
      }
    },
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      "proteinEffect": {
        "hgvs": "NP_862823.1:p.Tyr121LeufsTer?",
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      },
      "referenceSequence": "http://reg.genome.network/refseq/RS043899",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
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            "hgvs": "ENST00000334549.1:c.361dup"
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          "RefSeq": {
            "hgvs": "NM_181840.1:c.361dup"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000334650.1:p.Tyr121LeufsTer?"
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          "RefSeq": {
            "hgvs": "NP_862823.1:p.Tyr121LeufsTer?"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}