Canonical Allele Identifier: CA2748085522

Gene: AGT

Genomic Alleles

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

Transcript Alleles

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