Canonical Allele Identifier: CA414338148

Gene: AGTR2

Linked Data

• dbSNP Id: rs1922494274
• MyVariant Identifiers: chrX:g.115303883G>T (hg19) ; chrX:g.116172630G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116172630G>T , CM000685.2:g.116172630G>T	GRCh38
NC_000023.10:g.115303883G>T , CM000685.1:g.115303883G>T	GRCh37
NC_000023.9:g.115217911G>T	NCBI36
NG_016326.1:g.6926G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.350G>T MANE Select	ENSP00000360973.4:p.Cys117Phe
ENST00000680409.1:n.818G>T
ENST00000681852.1:c.350G>T	ENSP00000505750.1:p.Cys117Phe
ENST00000371906.4:c.350G>T	ENSP00000360973.4:p.Cys117Phe
NM_000686.4:c.350G>T	NP_000677.2:p.Cys117Phe
XM_011537533.1:c.350G>T	XP_011535835.1:p.Cys117Phe
NM_000686.5:c.350G>T MANE Select	NP_000677.2:p.Cys117Phe
NM_001385624.1:c.350G>T	NP_001372553.1:p.Cys117Phe