Canonical Allele Identifier: CA1226666343
Gene: AGT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230702420C= , CM000663.2:g.230702420C= GRCh38
NC_000001.10:g.230838166C= , CM000663.1:g.230838166C= GRCh37
NC_000001.9:g.228904789C= NCBI36
NG_008836.1:g.17171G=
NG_008836.2:g.17171G=

Transcript Alleles

HGVS Amino-acid change
ENST00000679738.1:c.*721G= ENSP00000505063.1:n.*721G=
ENST00000679802.1:c.*1611G= ENSP00000505184.1:n.*1611G=
ENST00000679854.1:n.6457G=
ENST00000680041.1:c.*721G= ENSP00000504866.1:n.*721G=
ENST00000680783.1:c.829+7575G= ENSP00000506329.1:n.829+7575G=
ENST00000681347.1:n.4258G=
ENST00000681514.1:c.*721G= ENSP00000505963.1:n.*721G=
ENST00000681772.1:c.*1646G= ENSP00000505829.1:n.*1646G=