Canonical Allele Identifier: CA1013238313

Gene: AGT

Linked Data

• dbSNP Id: rs1663370631
• gnomAD v3: 1-230705911-G-A
• gnomAD v4: 1-230705911-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230705911G>A , CM000663.2:g.230705911G>A	GRCh38
NC_000001.10:g.230841657G>A , CM000663.1:g.230841657G>A	GRCh37
NC_000001.9:g.228908280G>A	NCBI36
NG_008836.1:g.13680C>T
NG_008836.2:g.13680C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1097+22C>T MANE Select	ENSP00000355627.5:n.1097+22C>T
ENST00000679684.1:c.1097+22C>T	ENSP00000505981.1:n.1097+22C>T
ENST00000679738.1:c.1097+22C>T	ENSP00000505063.1:n.1097+22C>T
ENST00000679802.1:c.*556+22C>T	ENSP00000505184.1:n.*556+22C>T
ENST00000679854.1:n.5402+22C>T
ENST00000679957.1:c.1097+22C>T	ENSP00000506646.1:n.1097+22C>T
ENST00000680041.1:c.1097+22C>T	ENSP00000504866.1:n.1097+22C>T
ENST00000680783.1:c.829+4084C>T	ENSP00000506329.1:n.829+4084C>T
ENST00000681269.1:c.1097+22C>T	ENSP00000505985.1:n.1097+22C>T
ENST00000681347.1:n.1630C>T
ENST00000681514.1:c.1097+22C>T	ENSP00000505963.1:n.1097+22C>T
ENST00000681772.1:c.*18C>T	ENSP00000505829.1:n.*18C>T
ENST00000366667.4:c.1124+22C>T	ENSP00000355627.4:n.1124+22C>T
NM_000029.3:c.1124+22C>T	NP_000020.1:n.1124+22C>T
NM_000029.4:c.1124+22C>T	NP_000020.1:n.1124+22C>T
NM_001382817.3:c.1097+22C>T	NP_001369746.2:n.1097+22C>T
NM_001384479.1:c.1097+22C>T MANE Select	NP_001371408.1:n.1097+22C>T