Canonical Allele Identifier: CA2650971862

Gene: AGT

Linked Data

• gnomAD v4: 1-230714131-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714131G>T , CM000663.2:g.230714131G>T	GRCh38
NC_000001.10:g.230849877G>T , CM000663.1:g.230849877G>T	GRCh37
NC_000001.9:g.228916500G>T	NCBI36
NG_008836.1:g.5460C>A
NG_008836.2:g.5460C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000679684.1:c.-76C>A	ENSP00000505981.1:n.-76C>A
ENST00000679738.1:c.-76C>A	ENSP00000505063.1:n.-76C>A
ENST00000679802.1:c.-76C>A	ENSP00000505184.1:n.-76C>A
ENST00000679854.1:n.436C>A
ENST00000679957.1:c.-76C>A	ENSP00000506646.1:n.-76C>A
ENST00000680041.1:c.-201C>A	ENSP00000504866.1:n.-201C>A
ENST00000680783.1:c.-76C>A	ENSP00000506329.1:n.-76C>A
ENST00000681269.1:c.-30-3278C>A	ENSP00000505985.1:n.-30-3278C>A
ENST00000681347.1:n.436C>A
ENST00000681772.1:c.-76C>A	ENSP00000505829.1:n.-76C>A
ENST00000366667.4:c.-49C>A	ENSP00000355627.4:n.-49C>A
NM_000029.3:c.-49C>A	NP_000020.1:n.-49C>A
NM_001382817.3:c.-30-3278C>A	NP_001369746.2:n.-30-3278C>A