Connectathon 11 Snapshot

This page is part of the FHIR Specification (v1.2.0: STU 3 Draft). 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

This is the narrative for the resource. See also the XML or JSON format.

Generated Narrative with Details

id: example

type: DNA

variationID: rs587778247 (Details : {http://www.ncbi.nlm.nih.gov/projects/SNP code '587778247' = '??)

referenceSeq: ENSESTT00000085772.1 (Details : {http://www.ensembl.org code 'ENSESTT00000085772.1' = '??)

Coordinates

-ChromosomeStartEndGenomeBuild
*7 (Details )5522797655227977GRCh37 (Details )

species: Homo sapiens (Details : {SNOMED CT code '337915000' = '??)

observedAllele: T

referenceAllele: A

Repositories

-UrlNameVariantIdReadGroupSetId
*https://www.googleapis.com/genomics/v1beta2ga4ghA1A2B1B2

 

 

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.