Canonical Allele Identifier: CA2650971348

Gene: AGT

Linked Data

• gnomAD v4: 1-230709871-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230709871G>T , CM000663.2:g.230709871G>T	GRCh38
NC_000001.10:g.230845617G>T , CM000663.1:g.230845617G>T	GRCh37
NC_000001.9:g.228912240G>T	NCBI36
NG_008836.1:g.9720C>A
NG_008836.2:g.9720C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.829+124C>A MANE Select	ENSP00000355627.5:n.829+124C>A
ENST00000679684.1:c.829+124C>A	ENSP00000505981.1:n.829+124C>A
ENST00000679738.1:c.829+124C>A	ENSP00000505063.1:n.829+124C>A
ENST00000679802.1:c.829+124C>A	ENSP00000505184.1:n.829+124C>A
ENST00000679854.1:n.1464C>A
ENST00000679957.1:c.829+124C>A	ENSP00000506646.1:n.829+124C>A
ENST00000680041.1:c.829+124C>A	ENSP00000504866.1:n.829+124C>A
ENST00000680783.1:c.829+124C>A	ENSP00000506329.1:n.829+124C>A
ENST00000681269.1:c.829+124C>A	ENSP00000505985.1:n.829+124C>A
ENST00000681347.1:n.1340+124C>A
ENST00000681514.1:c.829+124C>A	ENSP00000505963.1:n.829+124C>A
ENST00000681772.1:c.829+124C>A	ENSP00000505829.1:n.829+124C>A
ENST00000366667.4:c.856+124C>A	ENSP00000355627.4:n.856+124C>A
NM_000029.3:c.856+124C>A	NP_000020.1:n.856+124C>A
NM_000029.4:c.856+124C>A	NP_000020.1:n.856+124C>A
NM_001382817.3:c.829+124C>A	NP_001369746.2:n.829+124C>A
NM_001384479.1:c.829+124C>A MANE Select	NP_001371408.1:n.829+124C>A