{
  "@context": "http://reg.genome.network/schema/allele.jsonld",
  "@id": "http://reg.genome.network/allele/CA2580593916",
  "communityStandardTitle": [
    "NM_000301.5(PLG):c.787+195G>C"
  ],
  "externalRecords": {
    "dbSNP": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/snp/783147",
        "rs": 783147
      }
    ]
  },
  "genomicAlleles": [
    {
      "chromosome": "6",
      "coordinates": [
        {
          "allele": "C",
          "end": 160716958,
          "referenceAllele": "G",
          "start": 160716957
        }
      ],
      "hgvs": [
        "NC_000006.12:g.160716958G>C",
        "CM000668.2:g.160716958G>C"
      ],
      "referenceGenome": "GRCh38",
      "referenceSequence": "http://reg.genome.network/refseq/RS000054"
    },
    {
      "chromosome": "6",
      "coordinates": [
        {
          "allele": "C",
          "end": 161137990,
          "referenceAllele": "G",
          "start": 161137989
        }
      ],
      "hgvs": [
        "NC_000006.11:g.161137990G>C",
        "CM000668.1:g.161137990G>C"
      ],
      "referenceGenome": "GRCh37",
      "referenceSequence": "http://reg.genome.network/refseq/RS000030"
    },
    {
      "chromosome": "6",
      "coordinates": [
        {
          "allele": "C",
          "end": 161057980,
          "referenceAllele": "G",
          "start": 161057979
        }
      ],
      "hgvs": [
        "NC_000006.10:g.161057980G>C"
      ],
      "referenceGenome": "NCBI36",
      "referenceSequence": "http://reg.genome.network/refseq/RS000006"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 19766,
          "referenceAllele": "G",
          "start": 19765
        }
      ],
      "hgvs": [
        "NG_016200.1:g.19766G>C",
        "LRG_571:g.19766G>C"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS003006"
    }
  ],
  "transcriptAlleles": [
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 94,
          "endIntronDirection": "-",
          "endIntronOffset": 5449,
          "referenceAllele": "G",
          "start": 94,
          "startIntronDirection": "-",
          "startIntronOffset": 5450
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009071",
      "geneNCBI_id": 5340,
      "geneSymbol": "PLG",
      "hgvs": [
        "ENST00000297289.9:c.50-5450G>C"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000516619.1:n.50-5450G>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS904350"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 949,
          "endIntronDirection": "+",
          "endIntronOffset": 195,
          "referenceAllele": "G",
          "start": 949,
          "startIntronDirection": "+",
          "startIntronOffset": 194
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009071",
      "geneNCBI_id": 5340,
      "geneSymbol": "PLG",
      "hgvs": [
        "ENST00000418964.2:c.838+195G>C"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000389424.2:n.838+195G>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS904746"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 850,
          "endIntronDirection": "+",
          "endIntronOffset": 195,
          "referenceAllele": "G",
          "start": 850,
          "startIntronDirection": "+",
          "startIntronOffset": 194
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009071",
      "geneNCBI_id": 5340,
      "geneSymbol": "PLG",
      "hgvs": [
        "ENST00000706906.1:c.787+195G>C"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000516618.1:n.787+195G>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS913251"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 848,
          "endIntronDirection": "+",
          "endIntronOffset": 195,
          "referenceAllele": "G",
          "start": 848,
          "startIntronDirection": "+",
          "startIntronOffset": 194
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009071",
      "geneNCBI_id": 5340,
      "geneSymbol": "PLG",
      "hgvs": [
        "ENST00000308192.14:c.787+195G>C"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000308938.9:n.787+195G>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS745445",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000308192.14:c.787+195G>C"
          },
          "RefSeq": {
            "hgvs": "NM_000301.5:c.787+195G>C"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000308938.9:n.787+195G>C"
          },
          "RefSeq": {
            "hgvs": "NP_000292.1:n.787+195G>C"
          }
        }
      }
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 94,
          "endIntronDirection": "-",
          "endIntronOffset": 5449,
          "referenceAllele": "G",
          "start": 94,
          "startIntronDirection": "-",
          "startIntronOffset": 5450
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009071",
      "geneNCBI_id": 5340,
      "geneSymbol": "PLG",
      "hgvs": [
        "ENST00000297289.8:n.95-5450G>C"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS254448"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 850,
          "endIntronDirection": "+",
          "endIntronOffset": 195,
          "referenceAllele": "G",
          "start": 850,
          "startIntronDirection": "+",
          "startIntronOffset": 194
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009071",
      "geneNCBI_id": 5340,
      "geneSymbol": "PLG",
      "hgvs": [
        "ENST00000308192.13:c.787+195G>C"
      ],
      "proteinEffect": {
        "hgvs": "ENSP00000308938.9:n.787+195G>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS256015"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 899,
          "endIntronDirection": "+",
          "endIntronOffset": 195,
          "referenceAllele": "G",
          "start": 899,
          "startIntronDirection": "+",
          "startIntronOffset": 194
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009071",
      "geneNCBI_id": 5340,
      "geneSymbol": "PLG",
      "hgvs": [
        "NM_000301.3:c.787+195G>C",
        "LRG_571t1:c.787+195G>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_000292.1:n.787+195G>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS006362"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 850,
          "endIntronDirection": "+",
          "endIntronOffset": 195,
          "referenceAllele": "G",
          "start": 850,
          "startIntronDirection": "+",
          "startIntronOffset": 194
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009071",
      "geneNCBI_id": 5340,
      "geneSymbol": "PLG",
      "hgvs": [
        "NM_000301.4:c.787+195G>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_000292.1:n.787+195G>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS674779"
    },
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 848,
          "endIntronDirection": "+",
          "endIntronOffset": 195,
          "referenceAllele": "G",
          "start": 848,
          "startIntronDirection": "+",
          "startIntronOffset": 194
        }
      ],
      "gene": "http://reg.genome.network/gene/GN009071",
      "geneNCBI_id": 5340,
      "geneSymbol": "PLG",
      "hgvs": [
        "NM_000301.5:c.787+195G>C"
      ],
      "proteinEffect": {
        "hgvs": "NP_000292.1:n.787+195G>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS710823",
      "MANE": {
        "maneVersion": "1.3",
        "maneStatus": "MANE Select",
        "nucleotide": {
          "Ensembl": {
            "hgvs": "ENST00000308192.14:c.787+195G>C"
          },
          "RefSeq": {
            "hgvs": "NM_000301.5:c.787+195G>C"
          }
        },
        "protein": {
          "Ensembl": {
            "hgvs": "ENSP00000308938.9:n.787+195G>C"
          },
          "RefSeq": {
            "hgvs": "NP_000292.1:n.787+195G>C"
          }
        }
      }
    }
  ],
  "type": "nucleotide"
}