Canonical Allele Identifier: CA2838180512

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.41043968G>T , CM000665.2:g.41043968G>T	GRCh38
NC_000003.11:g.41085459G>T , CM000665.1:g.41085459G>T	GRCh37
NC_000003.10:g.41060463G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940768.1:n.6C>A