Canonical Allele Identifier: CA345205804

Gene: AGT

Linked Data

• MyVariant Identifiers: chr1:g.230845801A>C (hg19) ; chr1:g.230710055A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710055A>C , CM000663.2:g.230710055A>C	GRCh38
NC_000001.10:g.230845801A>C , CM000663.1:g.230845801A>C	GRCh37
NC_000001.9:g.228912424A>C	NCBI36
NG_008836.1:g.9536T>G
NG_008836.2:g.9536T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.769T>G MANE Select	ENSP00000355627.5:p.Ser257Ala
ENST00000679684.1:c.769T>G	ENSP00000505981.1:p.Ser257Ala
ENST00000679738.1:c.769T>G	ENSP00000505063.1:p.Ser257Ala
ENST00000679802.1:c.769T>G	ENSP00000505184.1:p.Ser257Ala
ENST00000679854.1:n.1280T>G
ENST00000679957.1:c.769T>G	ENSP00000506646.1:p.Ser257Ala
ENST00000680041.1:c.769T>G	ENSP00000504866.1:p.Ser257Ala
ENST00000680783.1:c.769T>G	ENSP00000506329.1:p.Ser257Ala
ENST00000681269.1:c.769T>G	ENSP00000505985.1:p.Ser257Ala
ENST00000681347.1:n.1280T>G
ENST00000681514.1:c.769T>G	ENSP00000505963.1:p.Ser257Ala
ENST00000681772.1:c.769T>G	ENSP00000505829.1:p.Ser257Ala
ENST00000366667.4:c.796T>G	ENSP00000355627.4:p.Ser266Ala
NM_000029.3:c.796T>G	NP_000020.1:p.Ser266Ala
NM_000029.4:c.796T>G	NP_000020.1:p.Ser266Ala
NM_001382817.3:c.769T>G	NP_001369746.2:p.Ser257Ala
NM_001384479.1:c.769T>G MANE Select	NP_001371408.1:p.Ser257Ala