Canonical Allele Identifier: CA38872612
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 1927847
ClinVar RCV Id: RCV002621905
dbSNP Id: rs61762541

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230710840C>T , CM000663.2:g.230710840C>T GRCh38
NC_000001.10:g.230846586C>T , CM000663.1:g.230846586C>T GRCh37
NC_000001.9:g.228913209C>T NCBI36
NG_008836.1:g.8751G>A
NG_008836.2:g.8751G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.-17G>A MANE Select ENSP00000355627.5:n.-17G>A
ENST00000679684.1:c.-17G>A ENSP00000505981.1:n.-17G>A
ENST00000679738.1:c.-17G>A ENSP00000505063.1:n.-17G>A
ENST00000679802.1:c.-17G>A ENSP00000505184.1:n.-17G>A
ENST00000679854.1:n.495G>A
ENST00000679957.1:c.-17G>A ENSP00000506646.1:n.-17G>A
ENST00000680041.1:c.-17G>A ENSP00000504866.1:n.-17G>A
ENST00000680783.1:c.-17G>A ENSP00000506329.1:n.-17G>A
ENST00000681269.1:c.-17G>A ENSP00000505985.1:n.-17G>A
ENST00000681347.1:n.495G>A
ENST00000681514.1:c.-17G>A ENSP00000505963.1:n.-17G>A
ENST00000681772.1:c.-17G>A ENSP00000505829.1:n.-17G>A
ENST00000366667.4:c.11G>A ENSP00000355627.4:p.Arg4Gln
NM_000029.3:c.11G>A NP_000020.1:p.Arg4Gln
NM_000029.4:c.11G>A NP_000020.1:p.Arg4Gln
NM_001382817.3:c.-17G>A NP_001369746.2:n.-17G>A
NM_001384479.1:c.-17G>A MANE Select NP_001371408.1:n.-17G>A