{
  "@context": "http://reg.genome.network/schema/allele.jsonld",
  "@id": "http://reg.genome.network/allele/CA14384742",
  "communityStandardTitle": [
    "NM_002737.3(PRKCA):c.*2389C>T"
  ],
  "externalRecords": {
    "MyVariantInfo_hg19": [
      {
        "@id": "http://myvariant.info/v1/variant/chr17:g.64802544C>T?assembly=hg19",
        "id": "chr17:g.64802544C>T"
      }
    ],
    "MyVariantInfo_hg38": [
      {
        "@id": "http://myvariant.info/v1/variant/chr17:g.66806426C>T?assembly=hg38",
        "id": "chr17:g.66806426C>T"
      }
    ],
    "dbSNP": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/snp/7342847",
        "rs": 7342847
      }
    ],
    "gnomAD_2": [
      {
        "@id": "http://gnomad.broadinstitute.org/variant/17-64802544-C-T?dataset=gnomad_r2_1",
        "id": "17-64802544-C-T",
        "variant": "17:64802544 C / T"
      }
    ],
    "gnomAD_3": [
      {
        "@id": "http://gnomad.broadinstitute.org/variant/17-66806426-C-T?dataset=gnomad_r3",
        "id": "17-66806426-C-T",
        "variant": "17:66806426 C / T"
      }
    ],
    "gnomAD_4": [
      {
        "@id": "http://gnomad.broadinstitute.org/variant/17-66806426-C-T?dataset=gnomad_r4",
        "id": "17-66806426-C-T",
        "variant": "17:66806426 C / T"
      }
    ]
  },
  "genomicAlleles": [
    {
      "chromosome": "17",
      "coordinates": [
        {
          "allele": "T",
          "end": 66806426,
          "referenceAllele": "C",
          "start": 66806425
        }
      ],
      "hgvs": [
        "NC_000017.11:g.66806426C>T",
        "CM000679.2:g.66806426C>T"
      ],
      "referenceGenome": "GRCh38",
      "referenceSequence": "http://reg.genome.network/refseq/RS000065"
    },
    {
      "chromosome": "17",
      "coordinates": [
        {
          "allele": "T",
          "end": 64802544,
          "referenceAllele": "C",
          "start": 64802543
        }
      ],
      "hgvs": [
        "NC_000017.10:g.64802544C>T",
        "CM000679.1:g.64802544C>T"
      ],
      "referenceGenome": "GRCh37",
      "referenceSequence": "http://reg.genome.network/refseq/RS000041"
    },
    {
      "chromosome": "17",
      "coordinates": [
        {
          "allele": "T",
          "end": 62233006,
          "referenceAllele": "C",
          "start": 62233005
        }
      ],
      "hgvs": [
        "NC_000017.9:g.62233006C>T"
      ],
      "referenceGenome": "NCBI36",
      "referenceSequence": "http://reg.genome.network/refseq/RS000017"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 508619,
          "referenceAllele": "C",
          "start": 508618
        }
      ],
      "hgvs": [
        "NG_012206.1:g.508619C>T"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS002288"
    }
  ],
  "transcriptAlleles": [
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 4647,
          "referenceAllele": "C",
          "start": 4646
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009393",
      "geneNCBI_id": 5578,
      "geneSymbol": "PRKCA",
      "hgvs": [
        "ENST00000413366.8:c.*2389C>T"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000408695.3:n.*2389C>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS754531",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000413366.8:c.*2389C>T"
          },
          "RefSeq": {
            "hgvs": "NM_002737.3:c.*2389C>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000408695.3:n.*2389C>T"
          },
          "RefSeq": {
            "hgvs": "NP_002728.2:n.*2389C>T"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 4434,
          "referenceAllele": "C",
          "start": 4433
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009393",
      "geneNCBI_id": 5578,
      "geneSymbol": "PRKCA",
      "hgvs": [
        "ENST00000413366.7:c.*2389C>T"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000408695.3:n.*2389C>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS283035"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 4452,
          "referenceAllele": "C",
          "start": 4451
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009393",
      "geneNCBI_id": 5578,
      "geneSymbol": "PRKCA",
      "hgvs": [
        "NM_002737.2:c.*2389C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_002728.1:n.*2389C>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS028023"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 4278,
          "referenceAllele": "C",
          "start": 4277
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009393",
      "geneNCBI_id": 5578,
      "geneSymbol": "PRKCA",
      "hgvs": [
        "XM_011524989.1:c.*2389C>T"
      ],
      "proteinEffect": {
        "hgvs": "XP_011523291.1:n.*2389C>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS092108"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 4526,
          "referenceAllele": "C",
          "start": 4525
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009393",
      "geneNCBI_id": 5578,
      "geneSymbol": "PRKCA",
      "hgvs": [
        "XM_011524990.1:c.*2389C>T"
      ],
      "proteinEffect": {
        "hgvs": "XP_011523292.1:n.*2389C>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS092109"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 4283,
          "referenceAllele": "C",
          "start": 4282
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009393",
      "geneNCBI_id": 5578,
      "geneSymbol": "PRKCA",
      "hgvs": [
        "XM_017024837.1:c.*2389C>T"
      ],
      "proteinEffect": {
        "hgvs": "XP_016880326.1:n.*2389C>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS575304"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 5218,
          "referenceAllele": "C",
          "start": 5217
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009393",
      "geneNCBI_id": 5578,
      "geneSymbol": "PRKCA",
      "hgvs": [
        "XM_024450829.1:c.*2389C>T"
      ],
      "proteinEffect": {
        "hgvs": "XP_024306597.1:n.*2389C>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS584359"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 4300,
          "referenceAllele": "C",
          "start": 4299
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009393",
      "geneNCBI_id": 5578,
      "geneSymbol": "PRKCA",
      "hgvs": [
        "XM_024450830.1:c.*2389C>T"
      ],
      "proteinEffect": {
        "hgvs": "XP_024306598.1:n.*2389C>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS584360"
    },
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 4647,
          "referenceAllele": "C",
          "start": 4646
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009393",
      "geneNCBI_id": 5578,
      "geneSymbol": "PRKCA",
      "hgvs": [
        "NM_002737.3:c.*2389C>T"
      ],
      "proteinEffect": {
        "hgvs": "NP_002728.2:n.*2389C>T"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS665682",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000413366.8:c.*2389C>T"
          },
          "RefSeq": {
            "hgvs": "NM_002737.3:c.*2389C>T"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000408695.3:n.*2389C>T"
          },
          "RefSeq": {
            "hgvs": "NP_002728.2:n.*2389C>T"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}