Canonical Allele Identifier: CA414339426

Gene: AGTR2

Linked Data

• MyVariant Identifiers: chrX:g.115304456T>G (hg19) ; chrX:g.116173203T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116173203T>G , CM000685.2:g.116173203T>G	GRCh38
NC_000023.10:g.115304456T>G , CM000685.1:g.115304456T>G	GRCh37
NC_000023.9:g.115218484T>G	NCBI36
NG_016326.1:g.7499T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.923T>G MANE Select	ENSP00000360973.4:p.Phe308Cys
ENST00000680409.1:n.1391T>G
ENST00000681852.1:c.923T>G	ENSP00000505750.1:p.Phe308Cys
ENST00000371906.4:c.923T>G	ENSP00000360973.4:p.Phe308Cys
NM_000686.4:c.923T>G	NP_000677.2:p.Phe308Cys
XM_011537533.1:c.923T>G	XP_011535835.1:p.Phe308Cys
NM_000686.5:c.923T>G MANE Select	NP_000677.2:p.Phe308Cys
NM_001385624.1:c.923T>G	NP_001372553.1:p.Phe308Cys