Canonical Allele Identifier: CA529690759

Gene: AGT

Linked Data

• dbSNP Id: rs953264803
• gnomAD v2: 1-230838257-T-A
• gnomAD v3: 1-230702511-T-A
• gnomAD v4: 1-230702511-T-A
• MyVariant Identifiers: chr1:g.230838257T>A (hg19) ; chr1:g.230702511T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702511T>A , CM000663.2:g.230702511T>A	GRCh38
NC_000001.10:g.230838257T>A , CM000663.1:g.230838257T>A	GRCh37
NC_000001.9:g.228904880T>A	NCBI36
NG_008836.1:g.17080A>T
NG_008836.2:g.17080A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000679738.1:c.*630A>T	ENSP00000505063.1:n.*630A>T
ENST00000679802.1:c.*1520A>T	ENSP00000505184.1:n.*1520A>T
ENST00000679854.1:n.6366A>T
ENST00000680041.1:c.*630A>T	ENSP00000504866.1:n.*630A>T
ENST00000680783.1:c.829+7484A>T	ENSP00000506329.1:n.829+7484A>T
ENST00000681347.1:n.4167A>T
ENST00000681514.1:c.*630A>T	ENSP00000505963.1:n.*630A>T
ENST00000681772.1:c.*1555A>T	ENSP00000505829.1:n.*1555A>T