Canonical Allele Identifier: CA732697719

Gene: AGT

Linked Data

• ClinVar Variation Id: 873936
• ClinVar RCV Id: RCV001096498
• dbSNP Id: rs1472269720
• gnomAD v3: 1-230702527-T-C
• gnomAD v4: 1-230702527-T-C
• MyVariant Identifiers: chr1:g.230838273T>C (hg19) ; chr1:g.230702527T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702527T>C , CM000663.2:g.230702527T>C	GRCh38
NC_000001.10:g.230838273T>C , CM000663.1:g.230838273T>C	GRCh37
NC_000001.9:g.228904896T>C	NCBI36
NG_008836.1:g.17064A>G
NG_008836.2:g.17064A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.*614A>G MANE Select	ENSP00000355627.5:n.*614A>G
ENST00000679738.1:c.*614A>G	ENSP00000505063.1:n.*614A>G
ENST00000679802.1:c.*1504A>G	ENSP00000505184.1:n.*1504A>G
ENST00000679854.1:n.6350A>G
ENST00000680041.1:c.*614A>G	ENSP00000504866.1:n.*614A>G
ENST00000680783.1:c.829+7468A>G	ENSP00000506329.1:n.829+7468A>G
ENST00000681269.1:c.*614A>G	ENSP00000505985.1:n.*614A>G
ENST00000681347.1:n.4151A>G
ENST00000681514.1:c.*614A>G	ENSP00000505963.1:n.*614A>G
ENST00000681772.1:c.*1539A>G	ENSP00000505829.1:n.*1539A>G
ENST00000366667.4:c.*614A>G	ENSP00000355627.4:n.*614A>G
NM_000029.3:c.*614A>G	NP_000020.1:n.*614A>G
NM_000029.4:c.*614A>G	NP_000020.1:n.*614A>G
NM_001382817.3:c.*614A>G	NP_001369746.2:n.*614A>G
NM_001384479.1:c.*614A>G MANE Select	NP_001371408.1:n.*614A>G