Canonical Allele Identifier: CA10609425

Gene: AGT

Linked Data

• ClinVar Variation Id: 296066
• ClinVar RCV Id: RCV000266691
• dbSNP Id: rs886046078
• gnomAD v3: 1-230702633-G-A
• gnomAD v4: 1-230702633-G-A
• MyVariant Identifiers: chr1:g.230838379G>A (hg19) ; chr1:g.230702633G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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