Canonical Allele Identifier: CA1800979862

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.88981192C= , CM000670.2:g.88981192C=	GRCh38
NC_000008.10:g.89993421C= , CM000670.1:g.89993421C=	GRCh37
NC_000008.9:g.90062537C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_002956667.1:n.179-99131G=