Canonical Allele Identifier: CA1226666404

Gene: AGT

Linked Data

• dbSNP Id: rs1289650697
• gnomAD v4: 1-230702647-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702647A>G , CM000663.2:g.230702647A>G	GRCh38
NC_000001.10:g.230838393A>G , CM000663.1:g.230838393A>G	GRCh37
NC_000001.9:g.228905016A>G	NCBI36
NG_008836.1:g.16944T>C
NG_008836.2:g.16944T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.*494T>C MANE Select	ENSP00000355627.5:n.*494T>C
ENST00000679738.1:c.*494T>C	ENSP00000505063.1:n.*494T>C
ENST00000679802.1:c.*1384T>C	ENSP00000505184.1:n.*1384T>C
ENST00000679854.1:n.6230T>C
ENST00000680041.1:c.*494T>C	ENSP00000504866.1:n.*494T>C
ENST00000680783.1:c.829+7348T>C	ENSP00000506329.1:n.829+7348T>C
ENST00000681269.1:c.*494T>C	ENSP00000505985.1:n.*494T>C
ENST00000681347.1:n.4031T>C
ENST00000681514.1:c.*494T>C	ENSP00000505963.1:n.*494T>C
ENST00000681772.1:c.*1419T>C	ENSP00000505829.1:n.*1419T>C
ENST00000366667.4:c.*494T>C	ENSP00000355627.4:n.*494T>C
NM_000029.3:c.*494T>C	NP_000020.1:n.*494T>C
NM_000029.4:c.*494T>C	NP_000020.1:n.*494T>C
NM_001382817.3:c.*494T>C	NP_001369746.2:n.*494T>C
NM_001384479.1:c.*494T>C MANE Select	NP_001371408.1:n.*494T>C