Canonical Allele Identifier: CA10610324
Gene: AGT HGNC NCBI

Linked Data

ClinVar Variation Id: 296090
dbSNP Id: rs5051

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230714126C>T , CM000663.2:g.230714126C>T GRCh38
NC_000001.10:g.230849872C>T , CM000663.1:g.230849872C>T GRCh37
NC_000001.9:g.228916495C>T NCBI36
NG_008836.1:g.5465G>A
NG_008836.2:g.5465G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000679684.1:c.-71G>A ENSP00000505981.1:p.=
ENST00000679738.1:c.-71G>A ENSP00000505063.1:p.=
ENST00000679802.1:c.-71G>A ENSP00000505184.1:p.=
ENST00000679854.1:n.441G>A
ENST00000679957.1:c.-71G>A ENSP00000506646.1:p.=
ENST00000680041.1:c.-196G>A ENSP00000504866.1:p.=
ENST00000680783.1:c.-71G>A ENSP00000506329.1:p.=
ENST00000681269.1:c.-30-3273G>A ENSP00000505985.1:p.=
ENST00000681347.1:n.441G>A
ENST00000681772.1:c.-71G>A ENSP00000505829.1:p.=
ENST00000366667.4:c.-44G>A ENSP00000355627.4:p.=
NM_000029.3:c.-44G>A NP_000020.1:p.=
NM_001382817.3:c.-30-3273G>A NP_001369746.2:p.=