Canonical Allele Identifier: CA2748085518
Gene: AGT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702419A>T , CM000663.2:g.230702419A>T GRCh38
NC_000001.10:g.230838165A>T , CM000663.1:g.230838165A>T GRCh37
NC_000001.9:g.228904788A>T NCBI36
NG_008836.1:g.17172T>A
NG_008836.2:g.17172T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000679738.1:c.*722T>A ENSP00000505063.1:n.*722T>A
ENST00000679802.1:c.*1612T>A ENSP00000505184.1:n.*1612T>A
ENST00000679854.1:n.6458T>A
ENST00000680041.1:c.*722T>A ENSP00000504866.1:n.*722T>A
ENST00000680783.1:c.829+7576T>A ENSP00000506329.1:n.829+7576T>A
ENST00000681347.1:n.4259T>A
ENST00000681514.1:c.*722T>A ENSP00000505963.1:n.*722T>A
ENST00000681772.1:c.*1647T>A ENSP00000505829.1:n.*1647T>A
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