Canonical Allele Identifier: CA1226666334
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702399A= , CM000663.2:g.230702399A= GRCh38
NC_000001.10:g.230838145A= , CM000663.1:g.230838145A= GRCh37
NC_000001.9:g.228904768A= NCBI36
NG_008836.1:g.17192T=
NG_008836.2:g.17192T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000679738.1:c.*742T= ENSP00000505063.1:n.*742T=
ENST00000679802.1:c.*1632T= ENSP00000505184.1:n.*1632T=
ENST00000679854.1:n.6478T=
ENST00000680041.1:c.*742T= ENSP00000504866.1:n.*742T=
ENST00000680783.1:c.829+7596T= ENSP00000506329.1:n.829+7596T=
ENST00000681347.1:n.4279T=
ENST00000681514.1:c.*742T= ENSP00000505963.1:n.*742T=
ENST00000681772.1:c.*1667T= ENSP00000505829.1:n.*1667T=