Canonical Allele Identifier: CA1672212021

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.149977706C= , CM000668.2:g.149977706C=	GRCh38
NC_000006.11:g.150298842C= , CM000668.1:g.150298842C=	GRCh37
NC_000006.10:g.150340535C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406262.1:n.236C=