Canonical Allele Identifier: CA1226666369
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702511T= , CM000663.2:g.230702511T= GRCh38
NC_000001.10:g.230838257T= , CM000663.1:g.230838257T= GRCh37
NC_000001.9:g.228904880T= NCBI36
NG_008836.1:g.17080A=
NG_008836.2:g.17080A=

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*630A= ENSP00000505063.1:n.*630A=
ENST00000679802.1:c.*1520A= ENSP00000505184.1:n.*1520A=
ENST00000679854.1:n.6366A=
ENST00000680041.1:c.*630A= ENSP00000504866.1:n.*630A=
ENST00000680783.1:c.829+7484A= ENSP00000506329.1:n.829+7484A=
ENST00000681347.1:n.4167A=
ENST00000681514.1:c.*630A= ENSP00000505963.1:n.*630A=
ENST00000681772.1:c.*1555A= ENSP00000505829.1:n.*1555A=