Canonical Allele Identifier: CA2650971882

Gene: AGT

Linked Data

• gnomAD v4: 1-230714155-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714155T>C , CM000663.2:g.230714155T>C	GRCh38
NC_000001.10:g.230849901T>C , CM000663.1:g.230849901T>C	GRCh37
NC_000001.9:g.228916524T>C	NCBI36
NG_008836.1:g.5436A>G
NG_008836.2:g.5436A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679684.1:c.-100A>G	ENSP00000505981.1:n.-100A>G
ENST00000679738.1:c.-100A>G	ENSP00000505063.1:n.-100A>G
ENST00000679802.1:c.-100A>G	ENSP00000505184.1:n.-100A>G
ENST00000679854.1:n.412A>G
ENST00000679957.1:c.-100A>G	ENSP00000506646.1:n.-100A>G
ENST00000680783.1:c.-100A>G	ENSP00000506329.1:n.-100A>G
ENST00000681269.1:c.-30-3302A>G	ENSP00000505985.1:n.-30-3302A>G
ENST00000681347.1:n.412A>G
ENST00000681772.1:c.-100A>G	ENSP00000505829.1:n.-100A>G
ENST00000366667.4:c.-73A>G	ENSP00000355627.4:n.-73A>G
NM_000029.3:c.-73A>G	NP_000020.1:n.-73A>G
NM_001382817.3:c.-30-3302A>G	NP_001369746.2:n.-30-3302A>G