R4 Ballot #1 #2 (Mixed Normative/Trial use)

This page is part of the FHIR Specification (v3.3.0: (v3.5.0: R4 Ballot 2). #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: R5 R4B R4 R3

Sequence-example-pgx-1

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 : example-pgx-1

type : dna

coordinateSystem : 0

patient : Patient/example

ReferenceSeqs

- Orientation ReferenceSeqId Strand WindowStart WindowEnd
* sense NG_007726.3 (Details : {http://www.ncbi.nlm.nih.gov/nuccore code 'NG_007726.3' = 'NG_007726.3) watson 55227970 55227980

Variants

- Start End ObservedAllele ReferenceAllele VariantPointer
* 55227976 55227977 G T Target Haplotype Observation

 

Other examples that reference this example:

  • Provenance/CWL Workflow

    •  

    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.