Canonical Allele Identifier: CA2698267242

Gene: AGT

Linked Data

• dbSNP Id: rs2102783799

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702397G>A , CM000663.2:g.230702397G>A	GRCh38
NC_000001.10:g.230838143G>A , CM000663.1:g.230838143G>A	GRCh37
NC_000001.9:g.228904766G>A	NCBI36
NG_008836.1:g.17194C>T
NG_008836.2:g.17194C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000679738.1:c.*744C>T	ENSP00000505063.1:n.*744C>T
ENST00000679802.1:c.*1634C>T	ENSP00000505184.1:n.*1634C>T
ENST00000679854.1:n.6480C>T
ENST00000680041.1:c.*744C>T	ENSP00000504866.1:n.*744C>T
ENST00000680783.1:c.829+7598C>T	ENSP00000506329.1:n.829+7598C>T
ENST00000681347.1:n.4281C>T
ENST00000681514.1:c.*744C>T	ENSP00000505963.1:n.*744C>T
ENST00000681772.1:c.*1669C>T	ENSP00000505829.1:n.*1669C>T