Canonical Allele Identifier: CA1226666367
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702493A= , CM000663.2:g.230702493A= GRCh38
NC_000001.10:g.230838239A= , CM000663.1:g.230838239A= GRCh37
NC_000001.9:g.228904862A= NCBI36
NG_008836.1:g.17098T=
NG_008836.2:g.17098T=

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*648T= ENSP00000505063.1:n.*648T=
ENST00000679802.1:c.*1538T= ENSP00000505184.1:n.*1538T=
ENST00000679854.1:n.6384T=
ENST00000680041.1:c.*648T= ENSP00000504866.1:n.*648T=
ENST00000680783.1:c.829+7502T= ENSP00000506329.1:n.829+7502T=
ENST00000681347.1:n.4185T=
ENST00000681514.1:c.*648T= ENSP00000505963.1:n.*648T=
ENST00000681772.1:c.*1573T= ENSP00000505829.1:n.*1573T=