Canonical Allele Identifier: CA1448217
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 429788
ClinVar RCV Id: RCV000493969
dbSNP Id: rs747815674

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230709994C>A , CM000663.2:g.230709994C>A GRCh38
NC_000001.10:g.230845740C>A , CM000663.1:g.230845740C>A GRCh37
NC_000001.9:g.228912363C>A NCBI36
NG_008836.1:g.9597G>T
NG_008836.2:g.9597G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.829+1G>T MANE Select ENSP00000355627.5:p.=
ENST00000679684.1:c.829+1G>T ENSP00000505981.1:p.=
ENST00000679738.1:c.829+1G>T ENSP00000505063.1:p.=
ENST00000679802.1:c.829+1G>T ENSP00000505184.1:p.=
ENST00000679854.1:n.1341G>T
ENST00000679957.1:c.829+1G>T ENSP00000506646.1:p.=
ENST00000680041.1:c.829+1G>T ENSP00000504866.1:p.=
ENST00000680783.1:c.829+1G>T ENSP00000506329.1:p.=
ENST00000681269.1:c.829+1G>T ENSP00000505985.1:p.=
ENST00000681347.1:n.1340+1G>T
ENST00000681514.1:c.829+1G>T ENSP00000505963.1:p.=
ENST00000681772.1:c.829+1G>T ENSP00000505829.1:p.=
ENST00000366667.4:c.856+1G>T ENSP00000355627.4:p.=
NM_000029.3:c.856+1G>T NP_000020.1:p.=
NM_000029.4:c.856+1G>T NP_000020.1:p.=
NM_001382817.3:c.829+1G>T NP_001369746.2:p.=
NM_001384479.1:c.829+1G>T MANE Select NP_001371408.1:p.=