{
  "@context": "http://reg.genome.network/schema/allele.jsonld",
  "@id": "http://reg.genome.network/allele/CA727804458",
  "communityStandardTitle": [
    "NC_000017.11:g.29376331C>G"
  ],
  "externalRecords": {
    "MyVariantInfo_hg19": [
      {
        "@id": "http://myvariant.info/v1/variant/chr17:g.27703349C>G?assembly=hg19",
        "id": "chr17:g.27703349C>G"
      }
    ],
    "MyVariantInfo_hg38": [
      {
        "@id": "http://myvariant.info/v1/variant/chr17:g.29376331C>G?assembly=hg38",
        "id": "chr17:g.29376331C>G"
      }
    ],
    "dbSNP": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/snp/2138852",
        "rs": 2138852
      }
    ]
  },
  "genomicAlleles": [
    {
      "chromosome": "17",
      "coordinates": [
        {
          "allele": "G",
          "end": 29376331,
          "referenceAllele": "C",
          "start": 29376330
        }
      ],
      "hgvs": [
        "NC_000017.11:g.29376331C>G",
        "CM000679.2:g.29376331C>G"
      ],
      "referenceGenome": "GRCh38",
      "referenceSequence": "http://reg.genome.network/refseq/RS000065"
    },
    {
      "chromosome": "17",
      "coordinates": [
        {
          "allele": "G",
          "end": 27703349,
          "referenceAllele": "C",
          "start": 27703348
        }
      ],
      "hgvs": [
        "NC_000017.10:g.27703349C>G",
        "CM000679.1:g.27703349C>G"
      ],
      "referenceGenome": "GRCh37",
      "referenceSequence": "http://reg.genome.network/refseq/RS000041"
    },
    {
      "chromosome": "17",
      "coordinates": [
        {
          "allele": "G",
          "end": 24727475,
          "referenceAllele": "C",
          "start": 24727474
        }
      ],
      "hgvs": [
        "NC_000017.9:g.24727475C>G"
      ],
      "referenceGenome": "NCBI36",
      "referenceSequence": "http://reg.genome.network/refseq/RS000017"
    }
  ],
  "transcriptAlleles": [
    {
      "coordinates": [
        {
          "allele": "C",
          "end": 1007,
          "endIntronDirection": "-",
          "endIntronOffset": 6025,
          "referenceAllele": "G",
          "start": 1007,
          "startIntronDirection": "-",
          "startIntronOffset": 6026
        }
      ],
      "hgvs": [
        "XM_011525588.1:c.1008-6026G>C"
      ],
      "proteinEffect": {
        "hgvs": "XP_011523890.1:n.1008-6026G>C"
      },
      "referenceSequence": "http://reg.genome.network/refseq/RS092707"
    }
  ],
  "type": "nucleotide"
}