Canonical Allele Identifier: CA694637147

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.105545890T>C , CM000675.2:g.105545890T>C	GRCh38
NC_000013.10:g.106198239T>C , CM000675.1:g.106198239T>C	GRCh37
NC_000013.9:g.104996240T>C	NCBI36