Canonical Allele Identifier: CA810627002

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.40414982T>C , CM000667.2:g.40414982T>C	GRCh38
NC_000005.9:g.40415084T>C , CM000667.1:g.40415084T>C	GRCh37
NC_000005.8:g.40450841T>C	NCBI36