<?xml version=“1.0” encoding=“UTF-8”?><Sequence xmlns=“hl7.org/fhir”>

<id value="example-pgx-1"/>
<text><status value="generated"/><div xmlns="http://www.w3.org/1999/xhtml"><p><b>Generated Narrative with Details</b></p><p><b>id</b>: example-pgx-1</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 &#39;NG_007726.3&#39; = &#39;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>55227976</td><td>55227977</td><td>G</td><td>T</td><td><a>Target Haplotype Observation</a></td></tr></table></div></text><type value="dna"/>
<coordinateSystem value="0"/>
<patient>
    <reference value="Patient/example"/>
</patient>
<referenceSeq>
    <referenceSeqId>
      <coding>
        <system value="http://www.ncbi.nlm.nih.gov/nuccore"/>
        <code value="NG_007726.3"/>
      </coding>
    </referenceSeqId>
    <strand value="1"/>
    <windowStart value="55227970"/>
    <windowEnd value="55227980"/>
</referenceSeq>
<variant>
    <start value="55227976"/>
    <end value="55227977"/>
    <observedAllele value="G"/>
    <referenceAllele value="T"/>
    <variantPointer>
      <reference value="Observation/example-haplotype1"/>
      <display value="Target Haplotype Observation"/>
    </variantPointer>
</variant>

</Sequence>