Canonical Allele Identifier: CA2748085538
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702608C>G , CM000663.2:g.230702608C>G GRCh38
NC_000001.10:g.230838354C>G , CM000663.1:g.230838354C>G GRCh37
NC_000001.9:g.228904977C>G NCBI36
NG_008836.1:g.16983G>C
NG_008836.2:g.16983G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.*533G>C MANE Select ENSP00000355627.5:n.*533G>C
ENST00000679738.1:c.*533G>C ENSP00000505063.1:n.*533G>C
ENST00000679802.1:c.*1423G>C ENSP00000505184.1:n.*1423G>C
ENST00000679854.1:n.6269G>C
ENST00000680041.1:c.*533G>C ENSP00000504866.1:n.*533G>C
ENST00000680783.1:c.829+7387G>C ENSP00000506329.1:n.829+7387G>C
ENST00000681269.1:c.*533G>C ENSP00000505985.1:n.*533G>C
ENST00000681347.1:n.4070G>C
ENST00000681514.1:c.*533G>C ENSP00000505963.1:n.*533G>C
ENST00000681772.1:c.*1458G>C ENSP00000505829.1:n.*1458G>C
ENST00000366667.4:c.*533G>C ENSP00000355627.4:n.*533G>C
NM_000029.3:c.*533G>C NP_000020.1:n.*533G>C
NM_000029.4:c.*533G>C NP_000020.1:n.*533G>C
NM_001382817.3:c.*533G>C NP_001369746.2:n.*533G>C
NM_001384479.1:c.*533G>C MANE Select NP_001371408.1:n.*533G>C