Canonical Allele Identifier: CA518449199

Gene: AGTR2

Linked Data

• MyVariant Identifiers: chrX:g.115303707A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116172454A>G , CM000685.2:g.116172454A>G	GRCh38
NC_000023.10:g.115303707A>G , CM000685.1:g.115303707A>G	GRCh37
NC_000023.9:g.115217735A>G	NCBI36
NG_016326.1:g.6750A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.174A>G MANE Select	ENSP00000360973.4:p.Gly58=
ENST00000680409.1:n.642A>G
ENST00000681852.1:c.174A>G	ENSP00000505750.1:p.Gly58=
ENST00000371906.4:c.174A>G	ENSP00000360973.4:p.Gly58=
NM_000686.4:c.174A>G	NP_000677.2:p.Gly58=
XM_011537533.1:c.174A>G	XP_011535835.1:p.Gly58=
NM_000686.5:c.174A>G MANE Select	NP_000677.2:p.Gly58=
NM_001385624.1:c.174A>G	NP_001372553.1:p.Gly58=