FHIR Release 3 (STU) R4 Ballot #2 (Mixed Normative/Trial use)

This page is part of the FHIR Specification (v3.0.2: STU 3). (v3.5.0: R4 Ballot #2). The current version which supercedes this version is 5.0.0 . For a full list of available versions, see the Directory of published versions . Page versions: R4B R4 R3

Sequence-graphic-example-4

Clinical Genomics Work Group Maturity Level : N/A Ballot Status : Informative Compartments : Not linked to any defined compartments

This is the narrative for the resource. See also the XML or , JSON or Turtle format. This example conforms to the profile Sequence .

Generated Narrative with Details

id : graphic-example-4

type : dna

coordinateSystem : 0

ReferenceSeqs

- Chromosome GenomeBuild Strand WindowStart WindowEnd
* chromosome 2 (Details : {http://hl7.org/fhir/chromosome-human {http://terminology.hl7.org/CodeSystem/chromosome-human code '2' = 'chromosome 2', given as 'chromosome 2'}) GRCh 38 1 watson 128273736 128273740

 

Other examples that reference this example:

  • Sequence/Sequence graph scenario 3

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    Usage note: every effort has been made to ensure that the examples are correct and useful, but they are not a normative part of the specification.