Canonical Allele Identifier: CA1181633468

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.94564035A= , CM000663.2:g.94564035A=	GRCh38
NC_000001.10:g.95029591A= , CM000663.1:g.95029591A=	GRCh37
NC_000001.9:g.94802179A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_001738161.1:n.461+422A=