Canonical Allele Identifier: CA732698309

Gene: AGT

Linked Data

• dbSNP Id: rs1458569473
• gnomAD v3: 1-230714124-CCCGG-C
• gnomAD v4: 1-230714124-CCCGG-C
• MyVariant Identifiers: chr1:g.230849871_230849874del (hg19) ; chr1:g.230714125_230714128del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230714129_230714132del , CM000663.2:g.230714129_230714132del	GRCh38
NC_000001.10:g.230849875_230849878del , CM000663.1:g.230849875_230849878del	GRCh37
NC_000001.9:g.228916498_228916501del	NCBI36
NG_008836.1:g.5463_5466del
NG_008836.2:g.5463_5466del

Transcript Alleles

HGVS	Amino-acid change
ENST00000679684.1:c.-73_-70del	ENSP00000505981.1:n.-73_-70del
ENST00000679738.1:c.-73_-70del	ENSP00000505063.1:n.-73_-70del
ENST00000679802.1:c.-73_-70del	ENSP00000505184.1:n.-73_-70del
ENST00000679854.1:n.439_442del
ENST00000679957.1:c.-73_-70del	ENSP00000506646.1:n.-73_-70del
ENST00000680041.1:c.-198_-195del	ENSP00000504866.1:n.-198_-195del
ENST00000680783.1:c.-73_-70del	ENSP00000506329.1:n.-73_-70del
ENST00000681269.1:c.-30-3275_-30-3272del	ENSP00000505985.1:n.-30-3275_-30-3272del
ENST00000681347.1:n.439_442del
ENST00000681772.1:c.-73_-70del	ENSP00000505829.1:n.-73_-70del
ENST00000366667.4:c.-46_-43del	ENSP00000355627.4:n.-46_-43del
NM_000029.3:c.-46_-43del	NP_000020.1:n.-46_-43del
NM_001382817.3:c.-30-3275_-30-3272del	NP_001369746.2:n.-30-3275_-30-3272del