Canonical Allele Identifier: CA1804794161

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.97269594G= , CM000670.2:g.97269594G=	GRCh38
NC_000008.10:g.98281822G= , CM000670.1:g.98281822G=	GRCh37
NC_000008.9:g.98350998G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_125390.1:n.471+149476C=