Canonical Allele Identifier: CA1013239150
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1663452728

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230708284T>C , CM000663.2:g.230708284T>C GRCh38
NC_000001.10:g.230844030T>C , CM000663.1:g.230844030T>C GRCh37
NC_000001.9:g.228910653T>C NCBI36
NG_008836.1:g.11307A>G
NG_008836.2:g.11307A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.829+1711A>G MANE Select ENSP00000355627.5:n.829+1711A>G
ENST00000679684.1:c.829+1711A>G ENSP00000505981.1:n.829+1711A>G
ENST00000679738.1:c.829+1711A>G ENSP00000505063.1:n.829+1711A>G
ENST00000679802.1:c.*288+823A>G ENSP00000505184.1:n.*288+823A>G
ENST00000679854.1:n.3051A>G
ENST00000679957.1:c.829+1711A>G ENSP00000506646.1:n.829+1711A>G
ENST00000680041.1:c.829+1711A>G ENSP00000504866.1:n.829+1711A>G
ENST00000680783.1:c.829+1711A>G ENSP00000506329.1:n.829+1711A>G
ENST00000681269.1:c.829+1711A>G ENSP00000505985.1:n.829+1711A>G
ENST00000681347.1:n.1340+1711A>G
ENST00000681514.1:c.829+1711A>G ENSP00000505963.1:n.829+1711A>G
ENST00000681772.1:c.829+1711A>G ENSP00000505829.1:n.829+1711A>G
ENST00000366667.4:c.856+1711A>G ENSP00000355627.4:n.856+1711A>G
NM_000029.3:c.856+1711A>G NP_000020.1:n.856+1711A>G
NM_000029.4:c.856+1711A>G NP_000020.1:n.856+1711A>G
NM_001382817.3:c.829+1711A>G NP_001369746.2:n.829+1711A>G
NM_001384479.1:c.829+1711A>G MANE Select NP_001371408.1:n.829+1711A>G