R4 Draft for Comment

This page is part of the FHIR Specification (v3.2.0: R4 Ballot 1). The current version which supercedes this version is 5.0.0. For a full list of available versions, see the Directory of published versions

Sequence-example

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 format. This example conforms to the profile Sequence.

Generated Narrative with Details

id: example

type: dna

coordinateSystem: 0

patient: Patient/example

ReferenceSeqs

-	ReferenceSeqId	Strand	WindowStart	WindowEnd
*	NC_000009.11 (Details : {http://www.ncbi.nlm.nih.gov/nuccore code 'NC_000009.11' = 'NC_000009.11)	1	22125500	22125510

Variants

-

Start

End

ObservedAllele

ReferenceAllele

*

22125503

22125504

C

G

Repositories

-

Type

Url

Name

VariantsetId

*

openapi

http://grch37.rest.ensembl.org/ga4gh/variants/3:rs1333049?content-type=application/json

GA4GH API

3:rs1333049

Other examples that reference this example:

Provenance/Biocompute Object

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.