Canonical Allele Identifier: CA1226666338
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702412G= , CM000663.2:g.230702412G= GRCh38
NC_000001.10:g.230838158G= , CM000663.1:g.230838158G= GRCh37
NC_000001.9:g.228904781G= NCBI36
NG_008836.1:g.17179C=
NG_008836.2:g.17179C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000679738.1:c.*729C= ENSP00000505063.1:n.*729C=
ENST00000679802.1:c.*1619C= ENSP00000505184.1:n.*1619C=
ENST00000679854.1:n.6465C=
ENST00000680041.1:c.*729C= ENSP00000504866.1:n.*729C=
ENST00000680783.1:c.829+7583C= ENSP00000506329.1:n.829+7583C=
ENST00000681347.1:n.4266C=
ENST00000681514.1:c.*729C= ENSP00000505963.1:n.*729C=
ENST00000681772.1:c.*1654C= ENSP00000505829.1:n.*1654C=