Canonical Allele Identifier: CA2650971836

Gene: AGT

Linked Data

• gnomAD v4: 1-230714108-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714108A>C , CM000663.2:g.230714108A>C	GRCh38
NC_000001.10:g.230849854A>C , CM000663.1:g.230849854A>C	GRCh37
NC_000001.9:g.228916477A>C	NCBI36
NG_008836.1:g.5483T>G
NG_008836.2:g.5483T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.-53T>G MANE Select	ENSP00000355627.5:n.-53T>G
ENST00000679684.1:c.-53T>G	ENSP00000505981.1:n.-53T>G
ENST00000679738.1:c.-53T>G	ENSP00000505063.1:n.-53T>G
ENST00000679802.1:c.-53T>G	ENSP00000505184.1:n.-53T>G
ENST00000679854.1:n.459T>G
ENST00000679957.1:c.-53T>G	ENSP00000506646.1:n.-53T>G
ENST00000680041.1:c.-178T>G	ENSP00000504866.1:n.-178T>G
ENST00000680783.1:c.-53T>G	ENSP00000506329.1:n.-53T>G
ENST00000681269.1:c.-30-3255T>G	ENSP00000505985.1:n.-30-3255T>G
ENST00000681347.1:n.459T>G
ENST00000681514.1:c.-140T>G	ENSP00000505963.1:n.-140T>G
ENST00000681772.1:c.-53T>G	ENSP00000505829.1:n.-53T>G
ENST00000366667.4:c.-26T>G	ENSP00000355627.4:n.-26T>G
NM_000029.3:c.-26T>G	NP_000020.1:n.-26T>G
NM_000029.4:c.-26T>G	NP_000020.1:n.-26T>G
NM_001382817.3:c.-30-3255T>G	NP_001369746.2:n.-30-3255T>G
NM_001384479.1:c.-53T>G MANE Select	NP_001371408.1:n.-53T>G