Canonical Allele Identifier: CA1139772902

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714337C= , CM000663.2:g.230714337C=	GRCh38
NC_000001.10:g.230850083C= , CM000663.1:g.230850083C=	GRCh37
NC_000001.9:g.228916706C=	NCBI36
NG_008836.1:g.5254G=
NG_008836.2:g.5254G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679684.1:c.-282G=	ENSP00000505981.1:n.-282G=
ENST00000679738.1:c.-282G=	ENSP00000505063.1:n.-282G=
ENST00000679802.1:c.-282G=	ENSP00000505184.1:n.-282G=
ENST00000679854.1:n.230G=
ENST00000679957.1:c.-282G=	ENSP00000506646.1:n.-282G=
ENST00000680783.1:c.-282G=	ENSP00000506329.1:n.-282G=
ENST00000681269.1:c.-30-3484G=	ENSP00000505985.1:n.-30-3484G=
ENST00000681347.1:n.230G=
ENST00000681772.1:c.-282G=	ENSP00000505829.1:n.-282G=
NM_000029.3:c.-255G=	NP_000020.1:n.-255G=
NM_001382817.3:c.-30-3484G=	NP_001369746.2:n.-30-3484G=