Canonical Allele Identifier: CA2650970439

Gene: AGT

Linked Data

• gnomAD v4: 1-230702534-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702534T>C , CM000663.2:g.230702534T>C	GRCh38
NC_000001.10:g.230838280T>C , CM000663.1:g.230838280T>C	GRCh37
NC_000001.9:g.228904903T>C	NCBI36
NG_008836.1:g.17057A>G
NG_008836.2:g.17057A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.*607A>G MANE Select	ENSP00000355627.5:n.*607A>G
ENST00000679738.1:c.*607A>G	ENSP00000505063.1:n.*607A>G
ENST00000679802.1:c.*1497A>G	ENSP00000505184.1:n.*1497A>G
ENST00000679854.1:n.6343A>G
ENST00000680041.1:c.*607A>G	ENSP00000504866.1:n.*607A>G
ENST00000680783.1:c.829+7461A>G	ENSP00000506329.1:n.829+7461A>G
ENST00000681269.1:c.*607A>G	ENSP00000505985.1:n.*607A>G
ENST00000681347.1:n.4144A>G
ENST00000681514.1:c.*607A>G	ENSP00000505963.1:n.*607A>G
ENST00000681772.1:c.*1532A>G	ENSP00000505829.1:n.*1532A>G
ENST00000366667.4:c.*607A>G	ENSP00000355627.4:n.*607A>G
NM_000029.3:c.*607A>G	NP_000020.1:n.*607A>G
NM_000029.4:c.*607A>G	NP_000020.1:n.*607A>G
NM_001382817.3:c.*607A>G	NP_001369746.2:n.*607A>G
NM_001384479.1:c.*607A>G MANE Select	NP_001371408.1:n.*607A>G