Canonical Allele Identifier: CA345206402

Gene: AGT

Linked Data

• ClinVar Variation Id: 2091998
• ClinVar RCV Id: RCV003008096
• dbSNP Id: rs1226490025
• MyVariant Identifiers: chr1:g.230846059C>T (hg19) ; chr1:g.230710313C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710313C>T , CM000663.2:g.230710313C>T	GRCh38
NC_000001.10:g.230846059C>T , CM000663.1:g.230846059C>T	GRCh37
NC_000001.9:g.228912682C>T	NCBI36
NG_008836.1:g.9278G>A
NG_008836.2:g.9278G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.511G>A MANE Select	ENSP00000355627.5:p.Val171Ile
ENST00000679684.1:c.511G>A	ENSP00000505981.1:p.Val171Ile
ENST00000679738.1:c.511G>A	ENSP00000505063.1:p.Val171Ile
ENST00000679802.1:c.511G>A	ENSP00000505184.1:p.Val171Ile
ENST00000679854.1:n.1022G>A
ENST00000679957.1:c.511G>A	ENSP00000506646.1:p.Val171Ile
ENST00000680041.1:c.511G>A	ENSP00000504866.1:p.Val171Ile
ENST00000680783.1:c.511G>A	ENSP00000506329.1:p.Val171Ile
ENST00000681269.1:c.511G>A	ENSP00000505985.1:p.Val171Ile
ENST00000681347.1:n.1022G>A
ENST00000681514.1:c.511G>A	ENSP00000505963.1:p.Val171Ile
ENST00000681772.1:c.511G>A	ENSP00000505829.1:p.Val171Ile
ENST00000366667.4:c.538G>A	ENSP00000355627.4:p.Val180Ile
NM_000029.3:c.538G>A	NP_000020.1:p.Val180Ile
NM_000029.4:c.538G>A	NP_000020.1:p.Val180Ile
NM_001382817.3:c.511G>A	NP_001369746.2:p.Val171Ile
NM_001384479.1:c.511G>A MANE Select	NP_001371408.1:p.Val171Ile