Canonical Allele Identifier: CA1226662122

Gene: AGT

Linked Data

• dbSNP Id: rs1571979331

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714134T>G , CM000663.2:g.230714134T>G	GRCh38
NC_000001.10:g.230849880T>G , CM000663.1:g.230849880T>G	GRCh37
NC_000001.9:g.228916503T>G	NCBI36
NG_008836.1:g.5457A>C
NG_008836.2:g.5457A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679684.1:c.-79A>C	ENSP00000505981.1:n.-79A>C
ENST00000679738.1:c.-79A>C	ENSP00000505063.1:n.-79A>C
ENST00000679802.1:c.-79A>C	ENSP00000505184.1:n.-79A>C
ENST00000679854.1:n.433A>C
ENST00000679957.1:c.-79A>C	ENSP00000506646.1:n.-79A>C
ENST00000680041.1:c.-204A>C	ENSP00000504866.1:n.-204A>C
ENST00000680783.1:c.-79A>C	ENSP00000506329.1:n.-79A>C
ENST00000681269.1:c.-30-3281A>C	ENSP00000505985.1:n.-30-3281A>C
ENST00000681347.1:n.433A>C
ENST00000681772.1:c.-79A>C	ENSP00000505829.1:n.-79A>C
ENST00000366667.4:c.-52A>C	ENSP00000355627.4:n.-52A>C
NM_000029.3:c.-52A>C	NP_000020.1:n.-52A>C
NM_001382817.3:c.-30-3281A>C	NP_001369746.2:n.-30-3281A>C