Canonical Allele Identifier: CA1139912183
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702512G= , CM000663.2:g.230702512G= GRCh38
NC_000001.10:g.230838258G= , CM000663.1:g.230838258G= GRCh37
NC_000001.9:g.228904881G= NCBI36
NG_008836.1:g.17079C=
NG_008836.2:g.17079C=

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*629C= ENSP00000505063.1:n.*629C=
ENST00000679802.1:c.*1519C= ENSP00000505184.1:n.*1519C=
ENST00000679854.1:n.6365C=
ENST00000680041.1:c.*629C= ENSP00000504866.1:n.*629C=
ENST00000680783.1:c.829+7483C= ENSP00000506329.1:n.829+7483C=
ENST00000681347.1:n.4166C=
ENST00000681514.1:c.*629C= ENSP00000505963.1:n.*629C=
ENST00000681772.1:c.*1554C= ENSP00000505829.1:n.*1554C=