Canonical Allele Identifier: CA732702836
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1414132535

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230709692G>T , CM000663.2:g.230709692G>T GRCh38
NC_000001.10:g.230845438G>T , CM000663.1:g.230845438G>T GRCh37
NC_000001.9:g.228912061G>T NCBI36
NG_008836.1:g.9899C>A
NG_008836.2:g.9899C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.829+303C>A MANE Select ENSP00000355627.5:n.829+303C>A
ENST00000679684.1:c.829+303C>A ENSP00000505981.1:n.829+303C>A
ENST00000679738.1:c.829+303C>A ENSP00000505063.1:n.829+303C>A
ENST00000679802.1:c.830-266C>A ENSP00000505184.1:n.830-266C>A
ENST00000679854.1:n.1643C>A
ENST00000679957.1:c.829+303C>A ENSP00000506646.1:n.829+303C>A
ENST00000680041.1:c.829+303C>A ENSP00000504866.1:n.829+303C>A
ENST00000680783.1:c.829+303C>A ENSP00000506329.1:n.829+303C>A
ENST00000681269.1:c.829+303C>A ENSP00000505985.1:n.829+303C>A
ENST00000681347.1:n.1340+303C>A
ENST00000681514.1:c.829+303C>A ENSP00000505963.1:n.829+303C>A
ENST00000681772.1:c.829+303C>A ENSP00000505829.1:n.829+303C>A
ENST00000366667.4:c.856+303C>A ENSP00000355627.4:n.856+303C>A
NM_000029.3:c.856+303C>A NP_000020.1:n.856+303C>A
NM_000029.4:c.856+303C>A NP_000020.1:n.856+303C>A
NM_001382817.3:c.829+303C>A NP_001369746.2:n.829+303C>A
NM_001384479.1:c.829+303C>A MANE Select NP_001371408.1:n.829+303C>A