Canonical Allele Identifier: CA38863002

Gene: AGT

Linked Data

• dbSNP Id: rs934987338
• gnomAD v2: 1-230838292-G-A
• gnomAD v3: 1-230702546-G-A
• gnomAD v4: 1-230702546-G-A
• MyVariant Identifiers: chr1:g.230838292G>A (hg19) ; chr1:g.230702546G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230702546G>A , CM000663.2:g.230702546G>A	GRCh38
NC_000001.10:g.230838292G>A , CM000663.1:g.230838292G>A	GRCh37
NC_000001.9:g.228904915G>A	NCBI36
NG_008836.1:g.17045C>T
NG_008836.2:g.17045C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.*595C>T MANE Select	ENSP00000355627.5:n.*595C>T
ENST00000679738.1:c.*595C>T	ENSP00000505063.1:n.*595C>T
ENST00000679802.1:c.*1485C>T	ENSP00000505184.1:n.*1485C>T
ENST00000679854.1:n.6331C>T
ENST00000680041.1:c.*595C>T	ENSP00000504866.1:n.*595C>T
ENST00000680783.1:c.829+7449C>T	ENSP00000506329.1:n.829+7449C>T
ENST00000681269.1:c.*595C>T	ENSP00000505985.1:n.*595C>T
ENST00000681347.1:n.4132C>T
ENST00000681514.1:c.*595C>T	ENSP00000505963.1:n.*595C>T
ENST00000681772.1:c.*1520C>T	ENSP00000505829.1:n.*1520C>T
ENST00000366667.4:c.*595C>T	ENSP00000355627.4:n.*595C>T
NM_000029.3:c.*595C>T	NP_000020.1:n.*595C>T
NM_000029.4:c.*595C>T	NP_000020.1:n.*595C>T
NM_001382817.3:c.*595C>T	NP_001369746.2:n.*595C>T
NM_001384479.1:c.*595C>T MANE Select	NP_001371408.1:n.*595C>T