Canonical Allele Identifier: CA1226668819
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230708303C= , CM000663.2:g.230708303C= GRCh38
NC_000001.10:g.230844049C= , CM000663.1:g.230844049C= GRCh37
NC_000001.9:g.228910672C= NCBI36
NG_008836.1:g.11288G=
NG_008836.2:g.11288G=

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.829+1692G= MANE Select ENSP00000355627.5:n.829+1692G=
ENST00000679684.1:c.829+1692G= ENSP00000505981.1:n.829+1692G=
ENST00000679738.1:c.829+1692G= ENSP00000505063.1:n.829+1692G=
ENST00000679802.1:c.*288+804G= ENSP00000505184.1:n.*288+804G=
ENST00000679854.1:n.3032G=
ENST00000679957.1:c.829+1692G= ENSP00000506646.1:n.829+1692G=
ENST00000680041.1:c.829+1692G= ENSP00000504866.1:n.829+1692G=
ENST00000680783.1:c.829+1692G= ENSP00000506329.1:n.829+1692G=
ENST00000681269.1:c.829+1692G= ENSP00000505985.1:n.829+1692G=
ENST00000681347.1:n.1340+1692G=
ENST00000681514.1:c.829+1692G= ENSP00000505963.1:n.829+1692G=
ENST00000681772.1:c.829+1692G= ENSP00000505829.1:n.829+1692G=
ENST00000366667.4:c.856+1692G= ENSP00000355627.4:n.856+1692G=
NM_000029.3:c.856+1692G= NP_000020.1:n.856+1692G=
NM_000029.4:c.856+1692G= NP_000020.1:n.856+1692G=
NM_001382817.3:c.829+1692G= NP_001369746.2:n.829+1692G=
NM_001384479.1:c.829+1692G= MANE Select NP_001371408.1:n.829+1692G=