Canonical Allele Identifier: CA1226666357

Gene: AGT

Linked Data

• dbSNP Id: rs1663260014

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702460dup , CM000663.2:g.230702460dup	GRCh38
NC_000001.10:g.230838206dup , CM000663.1:g.230838206dup	GRCh37
NC_000001.9:g.228904829dup	NCBI36
NG_008836.1:g.17133dup
NG_008836.2:g.17133dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679738.1:c.*683dup	ENSP00000505063.1:n.*683dup
ENST00000679802.1:c.*1573dup	ENSP00000505184.1:n.*1573dup
ENST00000679854.1:n.6419dup
ENST00000680041.1:c.*683dup	ENSP00000504866.1:n.*683dup
ENST00000680783.1:c.829+7537dup	ENSP00000506329.1:n.829+7537dup
ENST00000681347.1:n.4220dup
ENST00000681514.1:c.*683dup	ENSP00000505963.1:n.*683dup
ENST00000681772.1:c.*1608dup	ENSP00000505829.1:n.*1608dup