Canonical Allele Identifier: CA2748085515
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702403C>A , CM000663.2:g.230702403C>A GRCh38
NC_000001.10:g.230838149C>A , CM000663.1:g.230838149C>A GRCh37
NC_000001.9:g.228904772C>A NCBI36
NG_008836.1:g.17188G>T
NG_008836.2:g.17188G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*738G>T ENSP00000505063.1:n.*738G>T
ENST00000679802.1:c.*1628G>T ENSP00000505184.1:n.*1628G>T
ENST00000679854.1:n.6474G>T
ENST00000680041.1:c.*738G>T ENSP00000504866.1:n.*738G>T
ENST00000680783.1:c.829+7592G>T ENSP00000506329.1:n.829+7592G>T
ENST00000681347.1:n.4275G>T
ENST00000681514.1:c.*738G>T ENSP00000505963.1:n.*738G>T
ENST00000681772.1:c.*1663G>T ENSP00000505829.1:n.*1663G>T