Canonical Allele Identifier: CA1226666352
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702455C= , CM000663.2:g.230702455C= GRCh38
NC_000001.10:g.230838201C= , CM000663.1:g.230838201C= GRCh37
NC_000001.9:g.228904824C= NCBI36
NG_008836.1:g.17136G=
NG_008836.2:g.17136G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000679738.1:c.*686G= ENSP00000505063.1:n.*686G=
ENST00000679802.1:c.*1576G= ENSP00000505184.1:n.*1576G=
ENST00000679854.1:n.6422G=
ENST00000680041.1:c.*686G= ENSP00000504866.1:n.*686G=
ENST00000680783.1:c.829+7540G= ENSP00000506329.1:n.829+7540G=
ENST00000681347.1:n.4223G=
ENST00000681514.1:c.*686G= ENSP00000505963.1:n.*686G=
ENST00000681772.1:c.*1611G= ENSP00000505829.1:n.*1611G=