Canonical Allele Identifier: CA732698366

Gene: AGT

Linked Data

• dbSNP Id: rs1484456332
• gnomAD v3: 1-230714190-G-A
• gnomAD v4: 1-230714190-G-A
• MyVariant Identifiers: chr1:g.230849936G>A (hg19) ; chr1:g.230714190G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714190G>A , CM000663.2:g.230714190G>A	GRCh38
NC_000001.10:g.230849936G>A , CM000663.1:g.230849936G>A	GRCh37
NC_000001.9:g.228916559G>A	NCBI36
NG_008836.1:g.5401C>T
NG_008836.2:g.5401C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679684.1:c.-135C>T	ENSP00000505981.1:n.-135C>T
ENST00000679738.1:c.-135C>T	ENSP00000505063.1:n.-135C>T
ENST00000679802.1:c.-135C>T	ENSP00000505184.1:n.-135C>T
ENST00000679854.1:n.377C>T
ENST00000679957.1:c.-135C>T	ENSP00000506646.1:n.-135C>T
ENST00000680783.1:c.-135C>T	ENSP00000506329.1:n.-135C>T
ENST00000681269.1:c.-30-3337C>T	ENSP00000505985.1:n.-30-3337C>T
ENST00000681347.1:n.377C>T
ENST00000681772.1:c.-135C>T	ENSP00000505829.1:n.-135C>T
ENST00000366667.4:c.-108C>T	ENSP00000355627.4:n.-108C>T
NM_000029.3:c.-108C>T	NP_000020.1:n.-108C>T
NM_001382817.3:c.-30-3337C>T	NP_001369746.2:n.-30-3337C>T