Canonical Allele Identifier: CA38867660

Gene: AGT

Linked Data

• dbSNP Id: rs894014191
• gnomAD v4: 1-230705875-C-A
• MyVariant Identifiers: chr1:g.230841621C>A (hg19) ; chr1:g.230705875C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230705875C>A , CM000663.2:g.230705875C>A	GRCh38
NC_000001.10:g.230841621C>A , CM000663.1:g.230841621C>A	GRCh37
NC_000001.9:g.228908244C>A	NCBI36
NG_008836.1:g.13716G>T
NG_008836.2:g.13716G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.1097+58G>T MANE Select	ENSP00000355627.5:n.1097+58G>T
ENST00000679684.1:c.1097+58G>T	ENSP00000505981.1:n.1097+58G>T
ENST00000679738.1:c.1097+58G>T	ENSP00000505063.1:n.1097+58G>T
ENST00000679802.1:c.*556+58G>T	ENSP00000505184.1:n.*556+58G>T
ENST00000679854.1:n.5402+58G>T
ENST00000679957.1:c.1097+58G>T	ENSP00000506646.1:n.1097+58G>T
ENST00000680041.1:c.1097+58G>T	ENSP00000504866.1:n.1097+58G>T
ENST00000680783.1:c.829+4120G>T	ENSP00000506329.1:n.829+4120G>T
ENST00000681269.1:c.1097+58G>T	ENSP00000505985.1:n.1097+58G>T
ENST00000681347.1:n.1666G>T
ENST00000681514.1:c.1097+58G>T	ENSP00000505963.1:n.1097+58G>T
ENST00000681772.1:c.*54G>T	ENSP00000505829.1:n.*54G>T
ENST00000366667.4:c.1124+58G>T	ENSP00000355627.4:n.1124+58G>T
NM_000029.3:c.1124+58G>T	NP_000020.1:n.1124+58G>T
NM_000029.4:c.1124+58G>T	NP_000020.1:n.1124+58G>T
NM_001382817.3:c.1097+58G>T	NP_001369746.2:n.1097+58G>T
NM_001384479.1:c.1097+58G>T MANE Select	NP_001371408.1:n.1097+58G>T