Canonical Allele Identifier: CA1144951948

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702434T= , CM000663.2:g.230702434T=	GRCh38
NC_000001.10:g.230838180T= , CM000663.1:g.230838180T=	GRCh37
NC_000001.9:g.228904803T=	NCBI36
NG_008836.1:g.17157A=
NG_008836.2:g.17157A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000679738.1:c.*707A=	ENSP00000505063.1:n.*707A=
ENST00000679802.1:c.*1597A=	ENSP00000505184.1:n.*1597A=
ENST00000679854.1:n.6443A=
ENST00000680041.1:c.*707A=	ENSP00000504866.1:n.*707A=
ENST00000680783.1:c.829+7561A=	ENSP00000506329.1:n.829+7561A=
ENST00000681347.1:n.4244A=
ENST00000681514.1:c.*707A=	ENSP00000505963.1:n.*707A=
ENST00000681772.1:c.*1632A=	ENSP00000505829.1:n.*1632A=