Canonical Allele Identifier: CA2650970596

Gene: AGT

Linked Data

• gnomAD v4: 1-230702652-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702652C>G , CM000663.2:g.230702652C>G	GRCh38
NC_000001.10:g.230838398C>G , CM000663.1:g.230838398C>G	GRCh37
NC_000001.9:g.228905021C>G	NCBI36
NG_008836.1:g.16939G>C
NG_008836.2:g.16939G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.*489G>C MANE Select	ENSP00000355627.5:n.*489G>C
ENST00000679738.1:c.*489G>C	ENSP00000505063.1:n.*489G>C
ENST00000679802.1:c.*1379G>C	ENSP00000505184.1:n.*1379G>C
ENST00000679854.1:n.6225G>C
ENST00000680041.1:c.*489G>C	ENSP00000504866.1:n.*489G>C
ENST00000680783.1:c.829+7343G>C	ENSP00000506329.1:n.829+7343G>C
ENST00000681269.1:c.*489G>C	ENSP00000505985.1:n.*489G>C
ENST00000681347.1:n.4026G>C
ENST00000681514.1:c.*489G>C	ENSP00000505963.1:n.*489G>C
ENST00000681772.1:c.*1414G>C	ENSP00000505829.1:n.*1414G>C
ENST00000366667.4:c.*489G>C	ENSP00000355627.4:n.*489G>C
NM_000029.3:c.*489G>C	NP_000020.1:n.*489G>C
NM_000029.4:c.*489G>C	NP_000020.1:n.*489G>C
NM_001382817.3:c.*489G>C	NP_001369746.2:n.*489G>C
NM_001384479.1:c.*489G>C MANE Select	NP_001371408.1:n.*489G>C