Canonical Allele Identifier: CA1692167727

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.19003126G= , CM000669.2:g.19003126G=	GRCh38
NC_000007.13:g.19042749G= , CM000669.1:g.19042749G=	GRCh37
NC_000007.12:g.19009274G=	NCBI36
NG_023250.3:g.921178G=

Transcript Alleles

HGVS	Amino-acid Change
XR_927080.1:n.265-1879C=