Canonical Allele Identifier: CA10609419
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 296063
ClinVar RCV Id: RCV000390829
dbSNP Id: rs7079

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702585G>T , CM000663.2:g.230702585G>T GRCh38
NC_000001.10:g.230838331G>T , CM000663.1:g.230838331G>T GRCh37
NC_000001.9:g.228904954G>T NCBI36
NG_008836.1:g.17006C>A
NG_008836.2:g.17006C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.*556C>A MANE Select ENSP00000355627.5:p.=
ENST00000679738.1:c.*556C>A ENSP00000505063.1:p.=
ENST00000679802.1:c.*1446C>A ENSP00000505184.1:p.=
ENST00000679854.1:n.6292C>A
ENST00000680041.1:c.*556C>A ENSP00000504866.1:p.=
ENST00000680783.1:c.829+7410C>A ENSP00000506329.1:p.=
ENST00000681269.1:c.*556C>A ENSP00000505985.1:p.=
ENST00000681347.1:n.4093C>A
ENST00000681514.1:c.*556C>A ENSP00000505963.1:p.=
ENST00000681772.1:c.*1481C>A ENSP00000505829.1:p.=
ENST00000366667.4:c.*556C>A ENSP00000355627.4:p.=
NM_000029.3:c.*556C>A NP_000020.1:p.=
NM_000029.4:c.*556C>A NP_000020.1:p.=
NM_001382817.3:c.*556C>A NP_001369746.2:p.=
NM_001384479.1:c.*556C>A MANE Select NP_001371408.1:p.=