Canonical Allele Identifier: CA38865535

Gene: AGT

Linked Data

• dbSNP Id: rs539658128
• gnomAD v3: 1-230703180-G-A
• gnomAD v4: 1-230703180-G-A
• MyVariant Identifiers: chr1:g.230838926G>A (hg19) ; chr1:g.230703180G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703180G>A , CM000663.2:g.230703180G>A	GRCh38
NC_000001.10:g.230838926G>A , CM000663.1:g.230838926G>A	GRCh37
NC_000001.9:g.228905549G>A	NCBI36
NG_008836.1:g.16411C>T
NG_008836.2:g.16411C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1392C>T MANE Select	ENSP00000355627.5:p.His464=
ENST00000679738.1:c.1392C>T	ENSP00000505063.1:p.His464=
ENST00000679802.1:c.*851C>T	ENSP00000505184.1:n.*851C>T
ENST00000679854.1:n.5697C>T
ENST00000679957.1:c.1383C>T	ENSP00000506646.1:p.His461=
ENST00000680041.1:c.1392C>T	ENSP00000504866.1:p.His464=
ENST00000680783.1:c.829+6815C>T	ENSP00000506329.1:n.829+6815C>T
ENST00000681269.1:c.1392C>T	ENSP00000505985.1:p.His464=
ENST00000681347.1:n.3498C>T
ENST00000681514.1:c.1392C>T	ENSP00000505963.1:p.His464=
ENST00000681772.1:c.*886C>T	ENSP00000505829.1:n.*886C>T
ENST00000366667.4:c.1419C>T	ENSP00000355627.4:p.His473=
NM_000029.3:c.1419C>T	NP_000020.1:p.His473=
NM_000029.4:c.1419C>T	NP_000020.1:p.His473=
NM_001382817.3:c.1392C>T	NP_001369746.2:p.His464=
NM_001384479.1:c.1392C>T MANE Select	NP_001371408.1:p.His464=