Canonical Allele Identifier: CA38867739
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1012870153

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230705935G>A , CM000663.2:g.230705935G>A GRCh38
NC_000001.10:g.230841681G>A , CM000663.1:g.230841681G>A GRCh37
NC_000001.9:g.228908304G>A NCBI36
NG_008836.1:g.13656C>T
NG_008836.2:g.13656C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1095C>T MANE Select ENSP00000355627.5:p.Pro365=
ENST00000679684.1:c.1095C>T ENSP00000505981.1:p.Pro365=
ENST00000679738.1:c.1095C>T ENSP00000505063.1:p.Pro365=
ENST00000679802.1:c.*554C>T ENSP00000505184.1:n.*554C>T
ENST00000679854.1:n.5400C>T
ENST00000679957.1:c.1095C>T ENSP00000506646.1:p.Pro365=
ENST00000680041.1:c.1095C>T ENSP00000504866.1:p.Pro365=
ENST00000680783.1:c.829+4060C>T ENSP00000506329.1:n.829+4060C>T
ENST00000681269.1:c.1095C>T ENSP00000505985.1:p.Pro365=
ENST00000681347.1:n.1606C>T
ENST00000681514.1:c.1095C>T ENSP00000505963.1:p.Pro365=
ENST00000681772.1:c.1095C>T ENSP00000505829.1:p.Pro365=
ENST00000366667.4:c.1122C>T ENSP00000355627.4:p.Pro374=
NM_000029.3:c.1122C>T NP_000020.1:p.Pro374=
NM_000029.4:c.1122C>T NP_000020.1:p.Pro374=
NM_001382817.3:c.1095C>T NP_001369746.2:p.Pro365=
NM_001384479.1:c.1095C>T MANE Select NP_001371408.1:p.Pro365=