Canonical Allele Identifier: CA424036419
Gene: AGT HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.230841681G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230705935G>C , CM000663.2:g.230705935G>C GRCh38
NC_000001.10:g.230841681G>C , CM000663.1:g.230841681G>C GRCh37
NC_000001.9:g.228908304G>C NCBI36
NG_008836.1:g.13656C>G
NG_008836.2:g.13656C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366667.6:c.1095C>G MANE Select ENSP00000355627.5:p.Pro365=
ENST00000679684.1:c.1095C>G ENSP00000505981.1:p.Pro365=
ENST00000679738.1:c.1095C>G ENSP00000505063.1:p.Pro365=
ENST00000679802.1:c.*554C>G ENSP00000505184.1:p.=
ENST00000679854.1:n.5400C>G
ENST00000679957.1:c.1095C>G ENSP00000506646.1:p.Pro365=
ENST00000680041.1:c.1095C>G ENSP00000504866.1:p.Pro365=
ENST00000680783.1:c.829+4060C>G ENSP00000506329.1:p.=
ENST00000681269.1:c.1095C>G ENSP00000505985.1:p.Pro365=
ENST00000681347.1:n.1606C>G
ENST00000681514.1:c.1095C>G ENSP00000505963.1:p.Pro365=
ENST00000681772.1:c.1095C>G ENSP00000505829.1:p.Pro365=
ENST00000366667.4:c.1122C>G ENSP00000355627.4:p.Pro374=
NM_000029.3:c.1122C>G NP_000020.1:p.Pro374=
NM_000029.4:c.1122C>G NP_000020.1:p.Pro374=
NM_001382817.3:c.1095C>G NP_001369746.2:p.Pro365=
NM_001384479.1:c.1095C>G MANE Select NP_001371408.1:p.Pro365=