Canonical Allele Identifier: CA38871496

Gene: AGT

Linked Data

• dbSNP Id: rs143666867
• MyVariant Identifiers: chr1:g.230845914G>T (hg19) ; chr1:g.230710168G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710168G>T , CM000663.2:g.230710168G>T	GRCh38
NC_000001.10:g.230845914G>T , CM000663.1:g.230845914G>T	GRCh37
NC_000001.9:g.228912537G>T	NCBI36
NG_008836.1:g.9423C>A
NG_008836.2:g.9423C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.656C>A MANE Select	ENSP00000355627.5:p.Ala219Asp
ENST00000679684.1:c.656C>A	ENSP00000505981.1:p.Ala219Asp
ENST00000679738.1:c.656C>A	ENSP00000505063.1:p.Ala219Asp
ENST00000679802.1:c.656C>A	ENSP00000505184.1:p.Ala219Asp
ENST00000679854.1:n.1167C>A
ENST00000679957.1:c.656C>A	ENSP00000506646.1:p.Ala219Asp
ENST00000680041.1:c.656C>A	ENSP00000504866.1:p.Ala219Asp
ENST00000680783.1:c.656C>A	ENSP00000506329.1:p.Ala219Asp
ENST00000681269.1:c.656C>A	ENSP00000505985.1:p.Ala219Asp
ENST00000681347.1:n.1167C>A
ENST00000681514.1:c.656C>A	ENSP00000505963.1:p.Ala219Asp
ENST00000681772.1:c.656C>A	ENSP00000505829.1:p.Ala219Asp
ENST00000366667.4:c.683C>A	ENSP00000355627.4:p.Ala228Asp
NM_000029.3:c.683C>A	NP_000020.1:p.Ala228Asp
NM_000029.4:c.683C>A	NP_000020.1:p.Ala228Asp
NM_001382817.3:c.656C>A	NP_001369746.2:p.Ala219Asp
NM_001384479.1:c.656C>A MANE Select	NP_001371408.1:p.Ala219Asp