{
  "@context": "http://reg.genome.network/schema/allele.jsonld",
  "@id": "http://reg.genome.network/allele/CA241334369",
  "communityStandardTitle": [
    "NC_000012.12:g.95330153G>A"
  ],
  "externalRecords": {
    "MyVariantInfo_hg19": [
      {
        "@id": "http://myvariant.info/v1/variant/chr12:g.95723929G>A?assembly=hg19",
        "id": "chr12:g.95723929G>A"
      }
    ],
    "MyVariantInfo_hg38": [
      {
        "@id": "http://myvariant.info/v1/variant/chr12:g.95330153G>A?assembly=hg38",
        "id": "chr12:g.95330153G>A"
      }
    ],
    "dbSNP": [
      {
        "@id": "http://www.ncbi.nlm.nih.gov/snp/11107987",
        "rs": 11107987
      }
    ]
  },
  "genomicAlleles": [
    {
      "chromosome": "12",
      "coordinates": [
        {
          "allele": "A",
          "end": 95330153,
          "referenceAllele": "G",
          "start": 95330152
        }
      ],
      "hgvs": [
        "NC_000012.12:g.95330153G>A",
        "CM000674.2:g.95330153G>A"
      ],
      "referenceGenome": "GRCh38",
      "referenceSequence": "http://reg.genome.network/refseq/RS000060"
    },
    {
      "chromosome": "12",
      "coordinates": [
        {
          "allele": "A",
          "end": 95723929,
          "referenceAllele": "G",
          "start": 95723928
        }
      ],
      "hgvs": [
        "NC_000012.11:g.95723929G>A",
        "CM000674.1:g.95723929G>A"
      ],
      "referenceGenome": "GRCh37",
      "referenceSequence": "http://reg.genome.network/refseq/RS000036"
    },
    {
      "chromosome": "12",
      "coordinates": [
        {
          "allele": "A",
          "end": 94248060,
          "referenceAllele": "G",
          "start": 94248059
        }
      ],
      "hgvs": [
        "NC_000012.10:g.94248060G>A"
      ],
      "referenceGenome": "NCBI36",
      "referenceSequence": "http://reg.genome.network/refseq/RS000012"
    }
  ],
  "transcriptAlleles": [
    {
      "coordinates": [
        {
          "allele": "T",
          "end": 1058,
          "endIntronDirection": "+",
          "endIntronOffset": 10220,
          "referenceAllele": "C",
          "start": 1058,
          "startIntronDirection": "+",
          "startIntronOffset": 10219
        }
      ],
      "hgvs": [
        "ENST00000636165.1:n.1058+10220C>T"
      ],
      "referenceSequence": "http://reg.genome.network/refseq/RS762917"
    }
  ],
  "type": "nucleotide"
}