Canonical Allele Identifier: CA732697813

Gene: AGT

Linked Data

• dbSNP Id: rs886046078
• MyVariant Identifiers: chr1:g.230838379G>T (hg19) ; chr1:g.230702633G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702633G>T , CM000663.2:g.230702633G>T	GRCh38
NC_000001.10:g.230838379G>T , CM000663.1:g.230838379G>T	GRCh37
NC_000001.9:g.228905002G>T	NCBI36
NG_008836.1:g.16958C>A
NG_008836.2:g.16958C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.*508C>A MANE Select	ENSP00000355627.5:n.*508C>A
ENST00000679738.1:c.*508C>A	ENSP00000505063.1:n.*508C>A
ENST00000679802.1:c.*1398C>A	ENSP00000505184.1:n.*1398C>A
ENST00000679854.1:n.6244C>A
ENST00000680041.1:c.*508C>A	ENSP00000504866.1:n.*508C>A
ENST00000680783.1:c.829+7362C>A	ENSP00000506329.1:n.829+7362C>A
ENST00000681269.1:c.*508C>A	ENSP00000505985.1:n.*508C>A
ENST00000681347.1:n.4045C>A
ENST00000681514.1:c.*508C>A	ENSP00000505963.1:n.*508C>A
ENST00000681772.1:c.*1433C>A	ENSP00000505829.1:n.*1433C>A
ENST00000366667.4:c.*508C>A	ENSP00000355627.4:n.*508C>A
NM_000029.3:c.*508C>A	NP_000020.1:n.*508C>A
NM_000029.4:c.*508C>A	NP_000020.1:n.*508C>A
NM_001382817.3:c.*508C>A	NP_001369746.2:n.*508C>A
NM_001384479.1:c.*508C>A MANE Select	NP_001371408.1:n.*508C>A