Canonical Allele Identifier: CA423883458
Gene: AGT HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.230839942C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230704196C>G , CM000663.2:g.230704196C>G GRCh38
NC_000001.10:g.230839942C>G , CM000663.1:g.230839942C>G GRCh37
NC_000001.9:g.228906565C>G NCBI36
NG_008836.1:g.15395G>C
NG_008836.2:g.15395G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366667.6:c.1239G>C MANE Select ENSP00000355627.5:p.Gly413=
ENST00000679684.1:c.1239G>C ENSP00000505981.1:p.Gly413=
ENST00000679738.1:c.1239G>C ENSP00000505063.1:p.Gly413=
ENST00000679802.1:c.*698G>C ENSP00000505184.1:n.*698G>C
ENST00000679854.1:n.5544G>C
ENST00000679957.1:c.1233+6G>C ENSP00000506646.1:n.1233+6G>C
ENST00000680041.1:c.1239G>C ENSP00000504866.1:p.Gly413=
ENST00000680783.1:c.829+5799G>C ENSP00000506329.1:n.829+5799G>C
ENST00000681269.1:c.1239G>C ENSP00000505985.1:p.Gly413=
ENST00000681347.1:n.3345G>C
ENST00000681514.1:c.1239G>C ENSP00000505963.1:p.Gly413=
ENST00000681772.1:c.*733G>C ENSP00000505829.1:n.*733G>C
ENST00000366667.4:c.1266G>C ENSP00000355627.4:p.Gly422=
NM_000029.3:c.1266G>C NP_000020.1:p.Gly422=
NM_000029.4:c.1266G>C NP_000020.1:p.Gly422=
NM_001382817.3:c.1239G>C NP_001369746.2:p.Gly413=
NM_001384479.1:c.1239G>C MANE Select NP_001371408.1:p.Gly413=