Canonical Allele Identifier: CA38866268

Gene: AGT

Linked Data

• dbSNP Id: rs557964080
• gnomAD v4: 1-230704199-C-A
• MyVariant Identifiers: chr1:g.230839945C>A (hg19) ; chr1:g.230704199C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704199C>A , CM000663.2:g.230704199C>A	GRCh38
NC_000001.10:g.230839945C>A , CM000663.1:g.230839945C>A	GRCh37
NC_000001.9:g.228906568C>A	NCBI36
NG_008836.1:g.15392G>T
NG_008836.2:g.15392G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1236G>T MANE Select	ENSP00000355627.5:p.Val412=
ENST00000679684.1:c.1236G>T	ENSP00000505981.1:p.Val412=
ENST00000679738.1:c.1236G>T	ENSP00000505063.1:p.Val412=
ENST00000679802.1:c.*695G>T	ENSP00000505184.1:n.*695G>T
ENST00000679854.1:n.5541G>T
ENST00000679957.1:c.1233+3G>T	ENSP00000506646.1:n.1233+3G>T
ENST00000680041.1:c.1236G>T	ENSP00000504866.1:p.Val412=
ENST00000680783.1:c.829+5796G>T	ENSP00000506329.1:n.829+5796G>T
ENST00000681269.1:c.1236G>T	ENSP00000505985.1:p.Val412=
ENST00000681347.1:n.3342G>T
ENST00000681514.1:c.1236G>T	ENSP00000505963.1:p.Val412=
ENST00000681772.1:c.*730G>T	ENSP00000505829.1:n.*730G>T
ENST00000366667.4:c.1263G>T	ENSP00000355627.4:p.Val421=
NM_000029.3:c.1263G>T	NP_000020.1:p.Val421=
NM_000029.4:c.1263G>T	NP_000020.1:p.Val421=
NM_001382817.3:c.1236G>T	NP_001369746.2:p.Val412=
NM_001384479.1:c.1236G>T MANE Select	NP_001371408.1:p.Val412=