Canonical Allele Identifier: CA10976126

Gene: AGT

Linked Data

• dbSNP Id: rs2478545
• gnomAD: 1:230844121 G / A
• MyVariant Identifiers: chr1:g.230844121G>A (hg19) ; chr1:g.230708375G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230708375G>A , CM000663.2:g.230708375G>A	GRCh38
NC_000001.10:g.230844121G>A , CM000663.1:g.230844121G>A	GRCh37
NC_000001.9:g.228910744G>A	NCBI36
NG_008836.1:g.11216C>T
NG_008836.2:g.11216C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366667.6:c.829+1620C>T MANE Select	ENSP00000355627.5:p.=
ENST00000679684.1:c.829+1620C>T	ENSP00000505981.1:p.=
ENST00000679738.1:c.829+1620C>T	ENSP00000505063.1:p.=
ENST00000679802.1:c.*288+732C>T	ENSP00000505184.1:p.=
ENST00000679854.1:n.2960C>T
ENST00000679957.1:c.829+1620C>T	ENSP00000506646.1:p.=
ENST00000680041.1:c.829+1620C>T	ENSP00000504866.1:p.=
ENST00000680783.1:c.829+1620C>T	ENSP00000506329.1:p.=
ENST00000681269.1:c.829+1620C>T	ENSP00000505985.1:p.=
ENST00000681347.1:n.1340+1620C>T
ENST00000681514.1:c.829+1620C>T	ENSP00000505963.1:p.=
ENST00000681772.1:c.829+1620C>T	ENSP00000505829.1:p.=
ENST00000366667.4:c.856+1620C>T	ENSP00000355627.4:p.=
NM_000029.3:c.856+1620C>T	NP_000020.1:p.=
NM_000029.4:c.856+1620C>T	NP_000020.1:p.=
NM_001382817.3:c.829+1620C>T	NP_001369746.2:p.=
NM_001384479.1:c.829+1620C>T MANE Select	NP_001371408.1:p.=