Canonical Allele Identifier: CA345202681

Gene: AGT

Linked Data

• dbSNP Id: rs1177936698
• gnomAD v4: 1-230703316-A-G
• MyVariant Identifiers: chr1:g.230839062A>G (hg19) ; chr1:g.230703316A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703316A>G , CM000663.2:g.230703316A>G	GRCh38
NC_000001.10:g.230839062A>G , CM000663.1:g.230839062A>G	GRCh37
NC_000001.9:g.228905685A>G	NCBI36
NG_008836.1:g.16275T>C
NG_008836.2:g.16275T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1256T>C MANE Select	ENSP00000355627.5:p.Ile419Thr
ENST00000679738.1:c.1256T>C	ENSP00000505063.1:p.Ile419Thr
ENST00000679802.1:c.*715T>C	ENSP00000505184.1:n.*715T>C
ENST00000679854.1:n.5561T>C
ENST00000679957.1:c.1247T>C	ENSP00000506646.1:p.Ile416Thr
ENST00000680041.1:c.1256T>C	ENSP00000504866.1:p.Ile419Thr
ENST00000680783.1:c.829+6679T>C	ENSP00000506329.1:n.829+6679T>C
ENST00000681269.1:c.1256T>C	ENSP00000505985.1:p.Ile419Thr
ENST00000681347.1:n.3362T>C
ENST00000681514.1:c.1256T>C	ENSP00000505963.1:p.Ile419Thr
ENST00000681772.1:c.*750T>C	ENSP00000505829.1:n.*750T>C
ENST00000366667.4:c.1283T>C	ENSP00000355627.4:p.Ile428Thr
NM_000029.3:c.1283T>C	NP_000020.1:p.Ile428Thr
NM_000029.4:c.1283T>C	NP_000020.1:p.Ile428Thr
NM_001382817.3:c.1256T>C	NP_001369746.2:p.Ile419Thr
NM_001384479.1:c.1256T>C MANE Select	NP_001371408.1:p.Ile419Thr