{

"resourceType": "Sequence",
"id": "example-pgx-2",
"text": {
  "status": "generated",
  "div": "<div xmlns=\"http://www.w3.org/1999/xhtml\"><p><b>Generated Narrative with Details</b></p><p><b>id</b>: example-pgx-2</p><p><b>type</b>: dna</p><p><b>coordinateSystem</b>: 0</p><p><b>patient</b>: <a>Patient/example</a></p><h3>ReferenceSeqs</h3><table><tr><td>-</td><td><b>ReferenceSeqId</b></td><td><b>Strand</b></td><td><b>WindowStart</b></td><td><b>WindowEnd</b></td></tr><tr><td>*</td><td>NG_007726.3 <span>(Details : {http://www.ncbi.nlm.nih.gov/nuccore code 'NG_007726.3' = 'NG_007726.3)</span></td><td>1</td><td>55227970</td><td>55227980</td></tr></table><h3>Variants</h3><table><tr><td>-</td><td><b>Start</b></td><td><b>End</b></td><td><b>ObservedAllele</b></td><td><b>ReferenceAllele</b></td><td><b>VariantPointer</b></td></tr><tr><td>*</td><td>55227978</td><td>55227979</td><td>G</td><td>T</td><td><a>Target Haplotype Observation</a></td></tr></table></div>"
},
"type": "dna",
"coordinateSystem": 0,
"patient": {
  "reference": "Patient/example"
},
"referenceSeq": {
  "referenceSeqId": {
    "coding": [
      {
        "system": "http://www.ncbi.nlm.nih.gov/nuccore",
        "code": "NG_007726.3"
      }
    ]
  },
  "strand": 1,
  "windowStart": 55227970,
  "windowEnd": 55227980
},
"variant": [
  {
    "start": 55227978,
    "end": 55227979,
    "observedAllele": "G",
    "referenceAllele": "T",
    "variantPointer": {
      "reference": "Observation/example-haplotype2",
      "display": "Target Haplotype Observation"
    }
  }
]

}