Canonical Allele Identifier: CA2650970434

Gene: AGT

Linked Data

• gnomAD v4: 1-230702529-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702529G>T , CM000663.2:g.230702529G>T	GRCh38
NC_000001.10:g.230838275G>T , CM000663.1:g.230838275G>T	GRCh37
NC_000001.9:g.228904898G>T	NCBI36
NG_008836.1:g.17062C>A
NG_008836.2:g.17062C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.*612C>A MANE Select	ENSP00000355627.5:n.*612C>A
ENST00000679738.1:c.*612C>A	ENSP00000505063.1:n.*612C>A
ENST00000679802.1:c.*1502C>A	ENSP00000505184.1:n.*1502C>A
ENST00000679854.1:n.6348C>A
ENST00000680041.1:c.*612C>A	ENSP00000504866.1:n.*612C>A
ENST00000680783.1:c.829+7466C>A	ENSP00000506329.1:n.829+7466C>A
ENST00000681269.1:c.*612C>A	ENSP00000505985.1:n.*612C>A
ENST00000681347.1:n.4149C>A
ENST00000681514.1:c.*612C>A	ENSP00000505963.1:n.*612C>A
ENST00000681772.1:c.*1537C>A	ENSP00000505829.1:n.*1537C>A
ENST00000366667.4:c.*612C>A	ENSP00000355627.4:n.*612C>A
NM_000029.3:c.*612C>A	NP_000020.1:n.*612C>A
NM_000029.4:c.*612C>A	NP_000020.1:n.*612C>A
NM_001382817.3:c.*612C>A	NP_001369746.2:n.*612C>A
NM_001384479.1:c.*612C>A MANE Select	NP_001371408.1:n.*612C>A