Canonical Allele Identifier: CA38862952

Gene: AGT

Linked Data

• dbSNP Id: rs536665936
• gnomAD v3: 1-230702434-T-C
• gnomAD v4: 1-230702434-T-C
• MyVariant Identifiers: chr1:g.230838180T>C (hg19) ; chr1:g.230702434T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702434T>C , CM000663.2:g.230702434T>C	GRCh38
NC_000001.10:g.230838180T>C , CM000663.1:g.230838180T>C	GRCh37
NC_000001.9:g.228904803T>C	NCBI36
NG_008836.1:g.17157A>G
NG_008836.2:g.17157A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679738.1:c.*707A>G	ENSP00000505063.1:n.*707A>G
ENST00000679802.1:c.*1597A>G	ENSP00000505184.1:n.*1597A>G
ENST00000679854.1:n.6443A>G
ENST00000680041.1:c.*707A>G	ENSP00000504866.1:n.*707A>G
ENST00000680783.1:c.829+7561A>G	ENSP00000506329.1:n.829+7561A>G
ENST00000681347.1:n.4244A>G
ENST00000681514.1:c.*707A>G	ENSP00000505963.1:n.*707A>G
ENST00000681772.1:c.*1632A>G	ENSP00000505829.1:n.*1632A>G