Canonical Allele Identifier: CA518449139
Gene: AGTR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.115303608C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172355C>A , CM000685.2:g.116172355C>A GRCh38
NC_000023.10:g.115303608C>A , CM000685.1:g.115303608C>A GRCh37
NC_000023.9:g.115217636C>A NCBI36
NG_016326.1:g.6651C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371906.5:c.75C>A MANE Select ENSP00000360973.4:p.Ile25=
ENST00000680409.1:n.543C>A
ENST00000681852.1:c.75C>A ENSP00000505750.1:p.Ile25=
ENST00000371906.4:c.75C>A ENSP00000360973.4:p.Ile25=
NM_000686.4:c.75C>A NP_000677.2:p.Ile25=
XM_011537533.1:c.75C>A XP_011535835.1:p.Ile25=
NM_000686.5:c.75C>A MANE Select NP_000677.2:p.Ile25=
NM_001385624.1:c.75C>A NP_001372553.1:p.Ile25=