Canonical Allele Identifier: CA1800979872

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88981206C= , CM000670.2:g.88981206C=	GRCh38
NC_000008.10:g.89993435C= , CM000670.1:g.89993435C=	GRCh37
NC_000008.9:g.90062551C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_002956667.1:n.179-99145G=