Canonical Allele Identifier: CA423883544

Gene: AGT

Linked Data

• dbSNP Id: rs1663322360
• MyVariant Identifiers: chr1:g.230840044T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230704298T>A , CM000663.2:g.230704298T>A	GRCh38
NC_000001.10:g.230840044T>A , CM000663.1:g.230840044T>A	GRCh37
NC_000001.9:g.228906667T>A	NCBI36
NG_008836.1:g.15293A>T
NG_008836.2:g.15293A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1137A>T MANE Select	ENSP00000355627.5:p.Gly379=
ENST00000679684.1:c.1137A>T	ENSP00000505981.1:p.Gly379=
ENST00000679738.1:c.1137A>T	ENSP00000505063.1:p.Gly379=
ENST00000679802.1:c.*596A>T	ENSP00000505184.1:n.*596A>T
ENST00000679854.1:n.5442A>T
ENST00000679957.1:c.1137A>T	ENSP00000506646.1:p.Gly379=
ENST00000680041.1:c.1137A>T	ENSP00000504866.1:p.Gly379=
ENST00000680783.1:c.829+5697A>T	ENSP00000506329.1:n.829+5697A>T
ENST00000681269.1:c.1137A>T	ENSP00000505985.1:p.Gly379=
ENST00000681347.1:n.3243A>T
ENST00000681514.1:c.1137A>T	ENSP00000505963.1:p.Gly379=
ENST00000681772.1:c.*631A>T	ENSP00000505829.1:n.*631A>T
ENST00000366667.4:c.1164A>T	ENSP00000355627.4:p.Gly388=
NM_000029.3:c.1164A>T	NP_000020.1:p.Gly388=
NM_000029.4:c.1164A>T	NP_000020.1:p.Gly388=
NM_001382817.3:c.1137A>T	NP_001369746.2:p.Gly379=
NM_001384479.1:c.1137A>T MANE Select	NP_001371408.1:p.Gly379=