Canonical Allele Identifier: CA1448086
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 1982309
ClinVar RCV Id: RCV002785439
dbSNP Id: rs557964080

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230704199C>G , CM000663.2:g.230704199C>G GRCh38
NC_000001.10:g.230839945C>G , CM000663.1:g.230839945C>G GRCh37
NC_000001.9:g.228906568C>G NCBI36
NG_008836.1:g.15392G>C
NG_008836.2:g.15392G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.1236G>C MANE Select ENSP00000355627.5:p.Val412=
ENST00000679684.1:c.1236G>C ENSP00000505981.1:p.Val412=
ENST00000679738.1:c.1236G>C ENSP00000505063.1:p.Val412=
ENST00000679802.1:c.*695G>C ENSP00000505184.1:n.*695G>C
ENST00000679854.1:n.5541G>C
ENST00000679957.1:c.1233+3G>C ENSP00000506646.1:n.1233+3G>C
ENST00000680041.1:c.1236G>C ENSP00000504866.1:p.Val412=
ENST00000680783.1:c.829+5796G>C ENSP00000506329.1:n.829+5796G>C
ENST00000681269.1:c.1236G>C ENSP00000505985.1:p.Val412=
ENST00000681347.1:n.3342G>C
ENST00000681514.1:c.1236G>C ENSP00000505963.1:p.Val412=
ENST00000681772.1:c.*730G>C ENSP00000505829.1:n.*730G>C
ENST00000366667.4:c.1263G>C ENSP00000355627.4:p.Val421=
NM_000029.3:c.1263G>C NP_000020.1:p.Val421=
NM_000029.4:c.1263G>C NP_000020.1:p.Val421=
NM_001382817.3:c.1236G>C NP_001369746.2:p.Val412=
NM_001384479.1:c.1236G>C MANE Select NP_001371408.1:p.Val412=