Canonical Allele Identifier: CA518449149
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1602586215
gnomAD v4: X-116172370-G-A
MyVariant Identifiers: chrX:g.115303623G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172370G>A , CM000685.2:g.116172370G>A GRCh38
NC_000023.10:g.115303623G>A , CM000685.1:g.115303623G>A GRCh37
NC_000023.9:g.115217651G>A NCBI36
NG_016326.1:g.6666G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.90G>A MANE Select ENSP00000360973.4:p.Glu30=
ENST00000680409.1:n.558G>A
ENST00000681852.1:c.90G>A ENSP00000505750.1:p.Glu30=
ENST00000371906.4:c.90G>A ENSP00000360973.4:p.Glu30=
NM_000686.4:c.90G>A NP_000677.2:p.Glu30=
XM_011537533.1:c.90G>A XP_011535835.1:p.Glu30=
NM_000686.5:c.90G>A MANE Select NP_000677.2:p.Glu30=
NM_001385624.1:c.90G>A NP_001372553.1:p.Glu30=
Search 100 bp 5'
Search 100 bp 3'