Canonical Allele Identifier: CA1448402
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 876870
ClinVar RCV Id: RCV001102123
dbSNP Id: rs199476082

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230710823T>A , CM000663.2:g.230710823T>A GRCh38
NC_000001.10:g.230846569T>A , CM000663.1:g.230846569T>A GRCh37
NC_000001.9:g.228913192T>A NCBI36
NG_008836.1:g.8768A>T
NG_008836.2:g.8768A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1A>T
ENST00000679684.1:c.1A>T
ENST00000679738.1:c.1A>T
ENST00000679802.1:c.1A>T
ENST00000679854.1:n.512A>T
ENST00000679957.1:c.1A>T
ENST00000680041.1:c.1A>T
ENST00000680783.1:c.1A>T
ENST00000681269.1:c.1A>T
ENST00000681347.1:n.512A>T
ENST00000681514.1:c.1A>T
ENST00000681772.1:c.1A>T
ENST00000366667.4:c.28A>T ENSP00000355627.4:p.Met10Leu
NM_000029.3:c.28A>T NP_000020.1:p.Met10Leu
NM_000029.4:c.28A>T NP_000020.1:p.Met10Leu
NM_001382817.3:c.1A>T
NM_001384479.1:c.1A>T