Canonical Allele Identifier: CA1226662104

Gene: AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714129C= , CM000663.2:g.230714129C=	GRCh38
NC_000001.10:g.230849875C= , CM000663.1:g.230849875C=	GRCh37
NC_000001.9:g.228916498C=	NCBI36
NG_008836.1:g.5462G=
NG_008836.2:g.5462G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679684.1:c.-74G=	ENSP00000505981.1:n.-74G=
ENST00000679738.1:c.-74G=	ENSP00000505063.1:n.-74G=
ENST00000679802.1:c.-74G=	ENSP00000505184.1:n.-74G=
ENST00000679854.1:n.438G=
ENST00000679957.1:c.-74G=	ENSP00000506646.1:n.-74G=
ENST00000680041.1:c.-199G=	ENSP00000504866.1:n.-199G=
ENST00000680783.1:c.-74G=	ENSP00000506329.1:n.-74G=
ENST00000681269.1:c.-30-3276G=	ENSP00000505985.1:n.-30-3276G=
ENST00000681347.1:n.438G=
ENST00000681772.1:c.-74G=	ENSP00000505829.1:n.-74G=
ENST00000366667.4:c.-47G=	ENSP00000355627.4:n.-47G=
NM_000029.3:c.-47G=	NP_000020.1:n.-47G=
NM_001382817.3:c.-30-3276G=	NP_001369746.2:n.-30-3276G=