Canonical Allele Identifier: CA1226666366
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702491A= , CM000663.2:g.230702491A= GRCh38
NC_000001.10:g.230838237A= , CM000663.1:g.230838237A= GRCh37
NC_000001.9:g.228904860A= NCBI36
NG_008836.1:g.17100T=
NG_008836.2:g.17100T=

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*650T= ENSP00000505063.1:n.*650T=
ENST00000679802.1:c.*1540T= ENSP00000505184.1:n.*1540T=
ENST00000679854.1:n.6386T=
ENST00000680041.1:c.*650T= ENSP00000504866.1:n.*650T=
ENST00000680783.1:c.829+7504T= ENSP00000506329.1:n.829+7504T=
ENST00000681347.1:n.4187T=
ENST00000681514.1:c.*650T= ENSP00000505963.1:n.*650T=
ENST00000681772.1:c.*1575T= ENSP00000505829.1:n.*1575T=