Canonical Allele Identifier: CA10755149
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs2493134

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230713613T>C , CM000663.2:g.230713613T>C GRCh38
NC_000001.10:g.230849359T>C , CM000663.1:g.230849359T>C GRCh37
NC_000001.9:g.228915982T>C NCBI36
NG_008836.1:g.5978A>G
NG_008836.2:g.5978A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.-31+473A>G MANE Select ENSP00000355627.5:p.=
ENST00000679684.1:c.-31+473A>G ENSP00000505981.1:p.=
ENST00000679738.1:c.-31+473A>G ENSP00000505063.1:p.=
ENST00000679802.1:c.-31+473A>G ENSP00000505184.1:p.=
ENST00000679854.1:n.481+473A>G
ENST00000679957.1:c.-31+473A>G ENSP00000506646.1:p.=
ENST00000680041.1:c.-156+473A>G ENSP00000504866.1:p.=
ENST00000680783.1:c.-31+473A>G ENSP00000506329.1:p.=
ENST00000681269.1:c.-30-2760A>G ENSP00000505985.1:p.=
ENST00000681347.1:n.481+473A>G
ENST00000681514.1:c.-117-244A>G ENSP00000505963.1:p.=
ENST00000681772.1:c.-31+473A>G ENSP00000505829.1:p.=
ENST00000366667.4:c.-4+473A>G ENSP00000355627.4:p.=
NM_000029.3:c.-4+473A>G NP_000020.1:p.=
NM_000029.4:c.-4+473A>G NP_000020.1:p.=
NM_001382817.3:c.-30-2760A>G NP_001369746.2:p.=
NM_001384479.1:c.-31+473A>G MANE Select NP_001371408.1:p.=