Canonical Allele Identifier: CA1990185066

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89733564C= , CM000673.2:g.89733564C=	GRCh38
NC_000011.9:g.89466732C= , CM000673.1:g.89466732C=	GRCh37
NC_000011.8:g.89106380C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527668.1:n.2548C=