Canonical Allele Identifier: CA10609274

Gene: AGT

Linked Data

• ClinVar Variation Id: 296071
• ClinVar RCV Id: RCV000386467
• dbSNP Id: rs886046080
• gnomAD v2: 1-230838804-C-T
• gnomAD v3: 1-230703058-C-T
• gnomAD v4: 1-230703058-C-T
• MyVariant Identifiers: chr1:g.230838804C>T (hg19) ; chr1:g.230703058C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230703058C>T , CM000663.2:g.230703058C>T	GRCh38
NC_000001.10:g.230838804C>T , CM000663.1:g.230838804C>T	GRCh37
NC_000001.9:g.228905427C>T	NCBI36
NG_008836.1:g.16533G>A
NG_008836.2:g.16533G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.*83G>A MANE Select	ENSP00000355627.5:n.*83G>A
ENST00000679738.1:c.*83G>A	ENSP00000505063.1:n.*83G>A
ENST00000679802.1:c.*973G>A	ENSP00000505184.1:n.*973G>A
ENST00000679854.1:n.5819G>A
ENST00000680041.1:c.*83G>A	ENSP00000504866.1:n.*83G>A
ENST00000680783.1:c.829+6937G>A	ENSP00000506329.1:n.829+6937G>A
ENST00000681269.1:c.*83G>A	ENSP00000505985.1:n.*83G>A
ENST00000681347.1:n.3620G>A
ENST00000681514.1:c.*83G>A	ENSP00000505963.1:n.*83G>A
ENST00000681772.1:c.*1008G>A	ENSP00000505829.1:n.*1008G>A
ENST00000366667.4:c.*83G>A	ENSP00000355627.4:n.*83G>A
NM_000029.3:c.*83G>A	NP_000020.1:n.*83G>A
NM_000029.4:c.*83G>A	NP_000020.1:n.*83G>A
NM_001382817.3:c.*83G>A	NP_001369746.2:n.*83G>A
NM_001384479.1:c.*83G>A MANE Select	NP_001371408.1:n.*83G>A