Canonical Allele Identifier: CA518449131
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1556673665
MyVariant Identifiers: chrX:g.115303596G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172343G>A , CM000685.2:g.116172343G>A GRCh38
NC_000023.10:g.115303596G>A , CM000685.1:g.115303596G>A GRCh37
NC_000023.9:g.115217624G>A NCBI36
NG_016326.1:g.6639G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371906.5:c.63G>A MANE Select ENSP00000360973.4:p.Gly21=
ENST00000680409.1:n.531G>A
ENST00000681852.1:c.63G>A ENSP00000505750.1:p.Gly21=
ENST00000371906.4:c.63G>A ENSP00000360973.4:p.Gly21=
NM_000686.4:c.63G>A NP_000677.2:p.Gly21=
XM_011537533.1:c.63G>A XP_011535835.1:p.Gly21=
NM_000686.5:c.63G>A MANE Select NP_000677.2:p.Gly21=
NM_001385624.1:c.63G>A NP_001372553.1:p.Gly21=