Canonical Allele Identifier: CA38863038

Gene: AGT

Linked Data

• dbSNP Id: rs904996324
• gnomAD v4: 1-230702629-T-A
• MyVariant Identifiers: chr1:g.230838375T>A (hg19) ; chr1:g.230702629T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702629T>A , CM000663.2:g.230702629T>A	GRCh38
NC_000001.10:g.230838375T>A , CM000663.1:g.230838375T>A	GRCh37
NC_000001.9:g.228904998T>A	NCBI36
NG_008836.1:g.16962A>T
NG_008836.2:g.16962A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.*512A>T MANE Select	ENSP00000355627.5:n.*512A>T
ENST00000679738.1:c.*512A>T	ENSP00000505063.1:n.*512A>T
ENST00000679802.1:c.*1402A>T	ENSP00000505184.1:n.*1402A>T
ENST00000679854.1:n.6248A>T
ENST00000680041.1:c.*512A>T	ENSP00000504866.1:n.*512A>T
ENST00000680783.1:c.829+7366A>T	ENSP00000506329.1:n.829+7366A>T
ENST00000681269.1:c.*512A>T	ENSP00000505985.1:n.*512A>T
ENST00000681347.1:n.4049A>T
ENST00000681514.1:c.*512A>T	ENSP00000505963.1:n.*512A>T
ENST00000681772.1:c.*1437A>T	ENSP00000505829.1:n.*1437A>T
ENST00000366667.4:c.*512A>T	ENSP00000355627.4:n.*512A>T
NM_000029.3:c.*512A>T	NP_000020.1:n.*512A>T
NM_000029.4:c.*512A>T	NP_000020.1:n.*512A>T
NM_001382817.3:c.*512A>T	NP_001369746.2:n.*512A>T
NM_001384479.1:c.*512A>T MANE Select	NP_001371408.1:n.*512A>T