Canonical Allele Identifier: CA414339746

Gene: AGTR2

Linked Data

• dbSNP Id: rs781926713
• MyVariant Identifiers: chrX:g.115304597T>G (hg19) ; chrX:g.116173344T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116173344T>G , CM000685.2:g.116173344T>G	GRCh38
NC_000023.10:g.115304597T>G , CM000685.1:g.115304597T>G	GRCh37
NC_000023.9:g.115218625T>G	NCBI36
NG_016326.1:g.7640T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.1064T>G MANE Select	ENSP00000360973.4:p.Leu355Arg
ENST00000680409.1:n.1532T>G
ENST00000681852.1:c.1064T>G	ENSP00000505750.1:p.Leu355Arg
ENST00000371906.4:c.1064T>G	ENSP00000360973.4:p.Leu355Arg
NM_000686.4:c.1064T>G	NP_000677.2:p.Leu355Arg
XM_011537533.1:c.1064T>G	XP_011535835.1:p.Leu355Arg
NM_000686.5:c.1064T>G MANE Select	NP_000677.2:p.Leu355Arg
NM_001385624.1:c.1064T>G	NP_001372553.1:p.Leu355Arg