Canonical Allele Identifier: CA1804794376

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97269751G= , CM000670.2:g.97269751G=	GRCh38
NC_000008.10:g.98281979G= , CM000670.1:g.98281979G=	GRCh37
NC_000008.9:g.98351155G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125390.1:n.471+149319C=