Canonical Allele Identifier: CA1013237204
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1663260951

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702504T>A , CM000663.2:g.230702504T>A GRCh38
NC_000001.10:g.230838250T>A , CM000663.1:g.230838250T>A GRCh37
NC_000001.9:g.228904873T>A NCBI36
NG_008836.1:g.17087A>T
NG_008836.2:g.17087A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*637A>T ENSP00000505063.1:n.*637A>T
ENST00000679802.1:c.*1527A>T ENSP00000505184.1:n.*1527A>T
ENST00000679854.1:n.6373A>T
ENST00000680041.1:c.*637A>T ENSP00000504866.1:n.*637A>T
ENST00000680783.1:c.829+7491A>T ENSP00000506329.1:n.829+7491A>T
ENST00000681347.1:n.4174A>T
ENST00000681514.1:c.*637A>T ENSP00000505963.1:n.*637A>T
ENST00000681772.1:c.*1562A>T ENSP00000505829.1:n.*1562A>T