Canonical Allele Identifier: CA345202730

Gene: AGT

Linked Data

• MyVariant Identifiers: chr1:g.230839069T>G (hg19) ; chr1:g.230703323T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703323T>G , CM000663.2:g.230703323T>G	GRCh38
NC_000001.10:g.230839069T>G , CM000663.1:g.230839069T>G	GRCh37
NC_000001.9:g.228905692T>G	NCBI36
NG_008836.1:g.16268A>C
NG_008836.2:g.16268A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1249A>C MANE Select	ENSP00000355627.5:p.Asn417His
ENST00000679738.1:c.1249A>C	ENSP00000505063.1:p.Asn417His
ENST00000679802.1:c.*708A>C	ENSP00000505184.1:n.*708A>C
ENST00000679854.1:n.5554A>C
ENST00000679957.1:c.1240A>C	ENSP00000506646.1:p.Asn414His
ENST00000680041.1:c.1249A>C	ENSP00000504866.1:p.Asn417His
ENST00000680783.1:c.829+6672A>C	ENSP00000506329.1:n.829+6672A>C
ENST00000681269.1:c.1249A>C	ENSP00000505985.1:p.Asn417His
ENST00000681347.1:n.3355A>C
ENST00000681514.1:c.1249A>C	ENSP00000505963.1:p.Asn417His
ENST00000681772.1:c.*743A>C	ENSP00000505829.1:n.*743A>C
ENST00000366667.4:c.1276A>C	ENSP00000355627.4:p.Asn426His
NM_000029.3:c.1276A>C	NP_000020.1:p.Asn426His
NM_000029.4:c.1276A>C	NP_000020.1:p.Asn426His
NM_001382817.3:c.1249A>C	NP_001369746.2:p.Asn417His
NM_001384479.1:c.1249A>C MANE Select	NP_001371408.1:p.Asn417His