Canonical Allele Identifier: CA1140726465

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702398G= , CM000663.2:g.230702398G=	GRCh38
NC_000001.10:g.230838144G= , CM000663.1:g.230838144G=	GRCh37
NC_000001.9:g.228904767G=	NCBI36
NG_008836.1:g.17193C=
NG_008836.2:g.17193C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679738.1:c.*743C=	ENSP00000505063.1:n.*743C=
ENST00000679802.1:c.*1633C=	ENSP00000505184.1:n.*1633C=
ENST00000679854.1:n.6479C=
ENST00000680041.1:c.*743C=	ENSP00000504866.1:n.*743C=
ENST00000680783.1:c.829+7597C=	ENSP00000506329.1:n.829+7597C=
ENST00000681347.1:n.4280C=
ENST00000681514.1:c.*743C=	ENSP00000505963.1:n.*743C=
ENST00000681772.1:c.*1668C=	ENSP00000505829.1:n.*1668C=