Canonical Allele Identifier: CA345206101

Gene: AGT

Linked Data

• ClinVar Variation Id: 3097223
• ClinVar RCV Id: RCV004387057
• gnomAD v4: 1-230710199-G-A
• MyVariant Identifiers: chr1:g.230845945G>A (hg19) ; chr1:g.230710199G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710199G>A , CM000663.2:g.230710199G>A	GRCh38
NC_000001.10:g.230845945G>A , CM000663.1:g.230845945G>A	GRCh37
NC_000001.9:g.228912568G>A	NCBI36
NG_008836.1:g.9392C>T
NG_008836.2:g.9392C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.625C>T MANE Select	ENSP00000355627.5:p.His209Tyr
ENST00000679684.1:c.625C>T	ENSP00000505981.1:p.His209Tyr
ENST00000679738.1:c.625C>T	ENSP00000505063.1:p.His209Tyr
ENST00000679802.1:c.625C>T	ENSP00000505184.1:p.His209Tyr
ENST00000679854.1:n.1136C>T
ENST00000679957.1:c.625C>T	ENSP00000506646.1:p.His209Tyr
ENST00000680041.1:c.625C>T	ENSP00000504866.1:p.His209Tyr
ENST00000680783.1:c.625C>T	ENSP00000506329.1:p.His209Tyr
ENST00000681269.1:c.625C>T	ENSP00000505985.1:p.His209Tyr
ENST00000681347.1:n.1136C>T
ENST00000681514.1:c.625C>T	ENSP00000505963.1:p.His209Tyr
ENST00000681772.1:c.625C>T	ENSP00000505829.1:p.His209Tyr
ENST00000366667.4:c.652C>T	ENSP00000355627.4:p.His218Tyr
NM_000029.3:c.652C>T	NP_000020.1:p.His218Tyr
NM_000029.4:c.652C>T	NP_000020.1:p.His218Tyr
NM_001382817.3:c.625C>T	NP_001369746.2:p.His209Tyr
NM_001384479.1:c.625C>T MANE Select	NP_001371408.1:p.His209Tyr