Canonical Allele Identifier: CA423884096

Gene: AGT

Linked Data

• MyVariant Identifiers: chr1:g.230846585T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230710839T>G , CM000663.2:g.230710839T>G	GRCh38
NC_000001.10:g.230846585T>G , CM000663.1:g.230846585T>G	GRCh37
NC_000001.9:g.228913208T>G	NCBI36
NG_008836.1:g.8752A>C
NG_008836.2:g.8752A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366667.6:c.-16A>C MANE Select	ENSP00000355627.5:n.-16A>C
ENST00000679684.1:c.-16A>C	ENSP00000505981.1:n.-16A>C
ENST00000679738.1:c.-16A>C	ENSP00000505063.1:n.-16A>C
ENST00000679802.1:c.-16A>C	ENSP00000505184.1:n.-16A>C
ENST00000679854.1:n.496A>C
ENST00000679957.1:c.-16A>C	ENSP00000506646.1:n.-16A>C
ENST00000680041.1:c.-16A>C	ENSP00000504866.1:n.-16A>C
ENST00000680783.1:c.-16A>C	ENSP00000506329.1:n.-16A>C
ENST00000681269.1:c.-16A>C	ENSP00000505985.1:n.-16A>C
ENST00000681347.1:n.496A>C
ENST00000681514.1:c.-16A>C	ENSP00000505963.1:n.-16A>C
ENST00000681772.1:c.-16A>C	ENSP00000505829.1:n.-16A>C
ENST00000366667.4:c.12A>C	ENSP00000355627.4:p.Arg4=
NM_000029.3:c.12A>C	NP_000020.1:p.Arg4=
NM_000029.4:c.12A>C	NP_000020.1:p.Arg4=
NM_001382817.3:c.-16A>C	NP_001369746.2:n.-16A>C
NM_001384479.1:c.-16A>C MANE Select	NP_001371408.1:n.-16A>C