Canonical Allele Identifier: CA732697676

Gene: AGT

Linked Data

• dbSNP Id: rs1213303957
• gnomAD v4: 1-230702420-C-A
• MyVariant Identifiers: chr1:g.230838166C>A (hg19) ; chr1:g.230702420C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702420C>A , CM000663.2:g.230702420C>A	GRCh38
NC_000001.10:g.230838166C>A , CM000663.1:g.230838166C>A	GRCh37
NC_000001.9:g.228904789C>A	NCBI36
NG_008836.1:g.17171G>T
NG_008836.2:g.17171G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000679738.1:c.*721G>T	ENSP00000505063.1:n.*721G>T
ENST00000679802.1:c.*1611G>T	ENSP00000505184.1:n.*1611G>T
ENST00000679854.1:n.6457G>T
ENST00000680041.1:c.*721G>T	ENSP00000504866.1:n.*721G>T
ENST00000680783.1:c.829+7575G>T	ENSP00000506329.1:n.829+7575G>T
ENST00000681347.1:n.4258G>T
ENST00000681514.1:c.*721G>T	ENSP00000505963.1:n.*721G>T
ENST00000681772.1:c.*1646G>T	ENSP00000505829.1:n.*1646G>T