Canonical Allele Identifier: CA345201890

Gene: AGT

Linked Data

• dbSNP Id: rs143479528
• gnomAD v2: 1-230838903-G-C
• gnomAD v4: 1-230703157-G-C
• MyVariant Identifiers: chr1:g.230838903G>C (hg19) ; chr1:g.230703157G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703157G>C , CM000663.2:g.230703157G>C	GRCh38
NC_000001.10:g.230838903G>C , CM000663.1:g.230838903G>C	GRCh37
NC_000001.9:g.228905526G>C	NCBI36
NG_008836.1:g.16434C>G
NG_008836.2:g.16434C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.1415C>G MANE Select	ENSP00000355627.5:p.Pro472Arg
ENST00000679738.1:c.1415C>G	ENSP00000505063.1:p.Pro472Arg
ENST00000679802.1:c.*874C>G	ENSP00000505184.1:n.*874C>G
ENST00000679854.1:n.5720C>G
ENST00000679957.1:c.1406C>G	ENSP00000506646.1:p.Pro469Arg
ENST00000680041.1:c.1415C>G	ENSP00000504866.1:p.Pro472Arg
ENST00000680783.1:c.829+6838C>G	ENSP00000506329.1:n.829+6838C>G
ENST00000681269.1:c.1415C>G	ENSP00000505985.1:p.Pro472Arg
ENST00000681347.1:n.3521C>G
ENST00000681514.1:c.1415C>G	ENSP00000505963.1:p.Pro472Arg
ENST00000681772.1:c.*909C>G	ENSP00000505829.1:n.*909C>G
ENST00000366667.4:c.1442C>G	ENSP00000355627.4:p.Pro481Arg
NM_000029.3:c.1442C>G	NP_000020.1:p.Pro481Arg
NM_000029.4:c.1442C>G	NP_000020.1:p.Pro481Arg
NM_001382817.3:c.1415C>G	NP_001369746.2:p.Pro472Arg
NM_001384479.1:c.1415C>G MANE Select	NP_001371408.1:p.Pro472Arg