Canonical Allele Identifier: CA130189170

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157603105A>C , CM000667.2:g.157603105A>C	GRCh38
NC_000005.9:g.157030113A>C , CM000667.1:g.157030113A>C	GRCh37
NC_000005.8:g.156962691A>C	NCBI36