Canonical Allele Identifier: CA1226666355

Gene: AGT

Linked Data

• dbSNP Id: rs1663259916

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702456A>C , CM000663.2:g.230702456A>C	GRCh38
NC_000001.10:g.230838202A>C , CM000663.1:g.230838202A>C	GRCh37
NC_000001.9:g.228904825A>C	NCBI36
NG_008836.1:g.17135T>G
NG_008836.2:g.17135T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679738.1:c.*685T>G	ENSP00000505063.1:n.*685T>G
ENST00000679802.1:c.*1575T>G	ENSP00000505184.1:n.*1575T>G
ENST00000679854.1:n.6421T>G
ENST00000680041.1:c.*685T>G	ENSP00000504866.1:n.*685T>G
ENST00000680783.1:c.829+7539T>G	ENSP00000506329.1:n.829+7539T>G
ENST00000681347.1:n.4222T>G
ENST00000681514.1:c.*685T>G	ENSP00000505963.1:n.*685T>G
ENST00000681772.1:c.*1610T>G	ENSP00000505829.1:n.*1610T>G