Canonical Allele Identifier: CA1226666345

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702435C= , CM000663.2:g.230702435C=	GRCh38
NC_000001.10:g.230838181C= , CM000663.1:g.230838181C=	GRCh37
NC_000001.9:g.228904804C=	NCBI36
NG_008836.1:g.17156G=
NG_008836.2:g.17156G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679738.1:c.*706G=	ENSP00000505063.1:n.*706G=
ENST00000679802.1:c.*1596G=	ENSP00000505184.1:n.*1596G=
ENST00000679854.1:n.6442G=
ENST00000680041.1:c.*706G=	ENSP00000504866.1:n.*706G=
ENST00000680783.1:c.829+7560G=	ENSP00000506329.1:n.829+7560G=
ENST00000681347.1:n.4243G=
ENST00000681514.1:c.*706G=	ENSP00000505963.1:n.*706G=
ENST00000681772.1:c.*1631G=	ENSP00000505829.1:n.*1631G=