Canonical Allele Identifier: CA1448219
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 2175735
ClinVar RCV Id: RCV002602413
dbSNP Id: rs374407232

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230710007C>T , CM000663.2:g.230710007C>T GRCh38
NC_000001.10:g.230845753C>T , CM000663.1:g.230845753C>T GRCh37
NC_000001.9:g.228912376C>T NCBI36
NG_008836.1:g.9584G>A
NG_008836.2:g.9584G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.817G>A MANE Select ENSP00000355627.5:p.Val273Ile
ENST00000679684.1:c.817G>A ENSP00000505981.1:p.Val273Ile
ENST00000679738.1:c.817G>A ENSP00000505063.1:p.Val273Ile
ENST00000679802.1:c.817G>A ENSP00000505184.1:p.Val273Ile
ENST00000679854.1:n.1328G>A
ENST00000679957.1:c.817G>A ENSP00000506646.1:p.Val273Ile
ENST00000680041.1:c.817G>A ENSP00000504866.1:p.Val273Ile
ENST00000680783.1:c.817G>A ENSP00000506329.1:p.Val273Ile
ENST00000681269.1:c.817G>A ENSP00000505985.1:p.Val273Ile
ENST00000681347.1:n.1328G>A
ENST00000681514.1:c.817G>A ENSP00000505963.1:p.Val273Ile
ENST00000681772.1:c.817G>A ENSP00000505829.1:p.Val273Ile
ENST00000366667.4:c.844G>A ENSP00000355627.4:p.Val282Ile
NM_000029.3:c.844G>A NP_000020.1:p.Val282Ile
NM_000029.4:c.844G>A NP_000020.1:p.Val282Ile
NM_001382817.3:c.817G>A NP_001369746.2:p.Val273Ile
NM_001384479.1:c.817G>A MANE Select NP_001371408.1:p.Val273Ile