Canonical Allele Identifier: CA732697759

Gene: AGT

Linked Data

• dbSNP Id: rs1269245958
• MyVariant Identifiers: chr1:g.230838299A>T (hg19) ; chr1:g.230702553A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702553A>T , CM000663.2:g.230702553A>T	GRCh38
NC_000001.10:g.230838299A>T , CM000663.1:g.230838299A>T	GRCh37
NC_000001.9:g.228904922A>T	NCBI36
NG_008836.1:g.17038T>A
NG_008836.2:g.17038T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.*588T>A MANE Select	ENSP00000355627.5:n.*588T>A
ENST00000679738.1:c.*588T>A	ENSP00000505063.1:n.*588T>A
ENST00000679802.1:c.*1478T>A	ENSP00000505184.1:n.*1478T>A
ENST00000679854.1:n.6324T>A
ENST00000680041.1:c.*588T>A	ENSP00000504866.1:n.*588T>A
ENST00000680783.1:c.829+7442T>A	ENSP00000506329.1:n.829+7442T>A
ENST00000681269.1:c.*588T>A	ENSP00000505985.1:n.*588T>A
ENST00000681347.1:n.4125T>A
ENST00000681514.1:c.*588T>A	ENSP00000505963.1:n.*588T>A
ENST00000681772.1:c.*1513T>A	ENSP00000505829.1:n.*1513T>A
ENST00000366667.4:c.*588T>A	ENSP00000355627.4:n.*588T>A
NM_000029.3:c.*588T>A	NP_000020.1:n.*588T>A
NM_000029.4:c.*588T>A	NP_000020.1:n.*588T>A
NM_001382817.3:c.*588T>A	NP_001369746.2:n.*588T>A
NM_001384479.1:c.*588T>A MANE Select	NP_001371408.1:n.*588T>A