Canonical Allele Identifier: CA2748085537
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702597A>T , CM000663.2:g.230702597A>T GRCh38
NC_000001.10:g.230838343A>T , CM000663.1:g.230838343A>T GRCh37
NC_000001.9:g.228904966A>T NCBI36
NG_008836.1:g.16994T>A
NG_008836.2:g.16994T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.*544T>A MANE Select ENSP00000355627.5:n.*544T>A
ENST00000679738.1:c.*544T>A ENSP00000505063.1:n.*544T>A
ENST00000679802.1:c.*1434T>A ENSP00000505184.1:n.*1434T>A
ENST00000679854.1:n.6280T>A
ENST00000680041.1:c.*544T>A ENSP00000504866.1:n.*544T>A
ENST00000680783.1:c.829+7398T>A ENSP00000506329.1:n.829+7398T>A
ENST00000681269.1:c.*544T>A ENSP00000505985.1:n.*544T>A
ENST00000681347.1:n.4081T>A
ENST00000681514.1:c.*544T>A ENSP00000505963.1:n.*544T>A
ENST00000681772.1:c.*1469T>A ENSP00000505829.1:n.*1469T>A
ENST00000366667.4:c.*544T>A ENSP00000355627.4:n.*544T>A
NM_000029.3:c.*544T>A NP_000020.1:n.*544T>A
NM_000029.4:c.*544T>A NP_000020.1:n.*544T>A
NM_001382817.3:c.*544T>A NP_001369746.2:n.*544T>A
NM_001384479.1:c.*544T>A MANE Select NP_001371408.1:n.*544T>A