Canonical Allele Identifier: CA1226666348

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702441A= , CM000663.2:g.230702441A=	GRCh38
NC_000001.10:g.230838187A= , CM000663.1:g.230838187A=	GRCh37
NC_000001.9:g.228904810A=	NCBI36
NG_008836.1:g.17150T=
NG_008836.2:g.17150T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679738.1:c.*700T=	ENSP00000505063.1:n.*700T=
ENST00000679802.1:c.*1590T=	ENSP00000505184.1:n.*1590T=
ENST00000679854.1:n.6436T=
ENST00000680041.1:c.*700T=	ENSP00000504866.1:n.*700T=
ENST00000680783.1:c.829+7554T=	ENSP00000506329.1:n.829+7554T=
ENST00000681347.1:n.4237T=
ENST00000681514.1:c.*700T=	ENSP00000505963.1:n.*700T=
ENST00000681772.1:c.*1625T=	ENSP00000505829.1:n.*1625T=