Canonical Allele Identifier: CA808058121

Gene:

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177086459A>C , CM000667.2:g.177086459A>C	GRCh38
NC_000005.9:g.176513460A>C , CM000667.1:g.176513460A>C	GRCh37
NC_000005.8:g.176446066A>C	NCBI36
NG_012067.1:g.4540A>C

Transcript Alleles

HGVS	Amino-acid Change
XR_941273.1:n.321A>C