Canonical Allele Identifier: CA1226666350
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702446C= , CM000663.2:g.230702446C= GRCh38
NC_000001.10:g.230838192C= , CM000663.1:g.230838192C= GRCh37
NC_000001.9:g.228904815C= NCBI36
NG_008836.1:g.17145G=
NG_008836.2:g.17145G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000679738.1:c.*695G= ENSP00000505063.1:n.*695G=
ENST00000679802.1:c.*1585G= ENSP00000505184.1:n.*1585G=
ENST00000679854.1:n.6431G=
ENST00000680041.1:c.*695G= ENSP00000504866.1:n.*695G=
ENST00000680783.1:c.829+7549G= ENSP00000506329.1:n.829+7549G=
ENST00000681347.1:n.4232G=
ENST00000681514.1:c.*695G= ENSP00000505963.1:n.*695G=
ENST00000681772.1:c.*1620G= ENSP00000505829.1:n.*1620G=