Canonical Allele Identifier: CA2748085520
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702423C>A , CM000663.2:g.230702423C>A GRCh38
NC_000001.10:g.230838169C>A , CM000663.1:g.230838169C>A GRCh37
NC_000001.9:g.228904792C>A NCBI36
NG_008836.1:g.17168G>T
NG_008836.2:g.17168G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000679738.1:c.*718G>T ENSP00000505063.1:n.*718G>T
ENST00000679802.1:c.*1608G>T ENSP00000505184.1:n.*1608G>T
ENST00000679854.1:n.6454G>T
ENST00000680041.1:c.*718G>T ENSP00000504866.1:n.*718G>T
ENST00000680783.1:c.829+7572G>T ENSP00000506329.1:n.829+7572G>T
ENST00000681347.1:n.4255G>T
ENST00000681514.1:c.*718G>T ENSP00000505963.1:n.*718G>T
ENST00000681772.1:c.*1643G>T ENSP00000505829.1:n.*1643G>T