Canonical Allele Identifier: CA2650971872

Gene: AGT

Linked Data

• gnomAD v4: 1-230714145-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714145T>G , CM000663.2:g.230714145T>G	GRCh38
NC_000001.10:g.230849891T>G , CM000663.1:g.230849891T>G	GRCh37
NC_000001.9:g.228916514T>G	NCBI36
NG_008836.1:g.5446A>C
NG_008836.2:g.5446A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000679684.1:c.-90A>C	ENSP00000505981.1:n.-90A>C
ENST00000679738.1:c.-90A>C	ENSP00000505063.1:n.-90A>C
ENST00000679802.1:c.-90A>C	ENSP00000505184.1:n.-90A>C
ENST00000679854.1:n.422A>C
ENST00000679957.1:c.-90A>C	ENSP00000506646.1:n.-90A>C
ENST00000680041.1:c.-215A>C	ENSP00000504866.1:n.-215A>C
ENST00000680783.1:c.-90A>C	ENSP00000506329.1:n.-90A>C
ENST00000681269.1:c.-30-3292A>C	ENSP00000505985.1:n.-30-3292A>C
ENST00000681347.1:n.422A>C
ENST00000681772.1:c.-90A>C	ENSP00000505829.1:n.-90A>C
ENST00000366667.4:c.-63A>C	ENSP00000355627.4:n.-63A>C
NM_000029.3:c.-63A>C	NP_000020.1:n.-63A>C
NM_001382817.3:c.-30-3292A>C	NP_001369746.2:n.-30-3292A>C