Canonical Allele Identifier: CA2698179100

Gene: AGT

Linked Data

• dbSNP Id: rs1370903728

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702586G>C , CM000663.2:g.230702586G>C	GRCh38
NC_000001.10:g.230838332G>C , CM000663.1:g.230838332G>C	GRCh37
NC_000001.9:g.228904955G>C	NCBI36
NG_008836.1:g.17005C>G
NG_008836.2:g.17005C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.*555C>G MANE Select	ENSP00000355627.5:n.*555C>G
ENST00000679738.1:c.*555C>G	ENSP00000505063.1:n.*555C>G
ENST00000679802.1:c.*1445C>G	ENSP00000505184.1:n.*1445C>G
ENST00000679854.1:n.6291C>G
ENST00000680041.1:c.*555C>G	ENSP00000504866.1:n.*555C>G
ENST00000680783.1:c.829+7409C>G	ENSP00000506329.1:n.829+7409C>G
ENST00000681269.1:c.*555C>G	ENSP00000505985.1:n.*555C>G
ENST00000681347.1:n.4092C>G
ENST00000681514.1:c.*555C>G	ENSP00000505963.1:n.*555C>G
ENST00000681772.1:c.*1480C>G	ENSP00000505829.1:n.*1480C>G
ENST00000366667.4:c.*555C>G	ENSP00000355627.4:n.*555C>G
NM_000029.3:c.*555C>G	NP_000020.1:n.*555C>G
NM_000029.4:c.*555C>G	NP_000020.1:n.*555C>G
NM_001382817.3:c.*555C>G	NP_001369746.2:n.*555C>G
NM_001384479.1:c.*555C>G MANE Select	NP_001371408.1:n.*555C>G