Canonical Allele Identifier: CA1226666401
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702645C= , CM000663.2:g.230702645C= GRCh38
NC_000001.10:g.230838391C= , CM000663.1:g.230838391C= GRCh37
NC_000001.9:g.228905014C= NCBI36
NG_008836.1:g.16946G=
NG_008836.2:g.16946G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.*496G= MANE Select ENSP00000355627.5:n.*496G=
ENST00000679738.1:c.*496G= ENSP00000505063.1:n.*496G=
ENST00000679802.1:c.*1386G= ENSP00000505184.1:n.*1386G=
ENST00000679854.1:n.6232G=
ENST00000680041.1:c.*496G= ENSP00000504866.1:n.*496G=
ENST00000680783.1:c.829+7350G= ENSP00000506329.1:n.829+7350G=
ENST00000681269.1:c.*496G= ENSP00000505985.1:n.*496G=
ENST00000681347.1:n.4033G=
ENST00000681514.1:c.*496G= ENSP00000505963.1:n.*496G=
ENST00000681772.1:c.*1421G= ENSP00000505829.1:n.*1421G=
ENST00000366667.4:c.*496G= ENSP00000355627.4:n.*496G=
NM_000029.3:c.*496G= NP_000020.1:n.*496G=
NM_000029.4:c.*496G= NP_000020.1:n.*496G=
NM_001382817.3:c.*496G= NP_001369746.2:n.*496G=
NM_001384479.1:c.*496G= MANE Select NP_001371408.1:n.*496G=