Canonical Allele Identifier: CA10497252
Gene: AGTR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 389981
ClinVar RCV Id: RCV000425261
dbSNP Id: rs184954669
ExAC: X:115303831 T / C
gnomAD v2: X-115303831-T-C
gnomAD v3: X-116172578-T-C
gnomAD v4: X-116172578-T-C
MyVariant Identifiers: chrX:g.115303831T>C (hg19) chrX:g.115303831_115303832delinsCG (hg19) chrX:g.116172578T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172578T>C , CM000685.2:g.116172578T>C GRCh38
NC_000023.10:g.115303831T>C , CM000685.1:g.115303831T>C GRCh37
NC_000023.9:g.115217859T>C NCBI36
NG_016326.1:g.6874T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.298T>C MANE Select ENSP00000360973.4:p.Trp100Arg
ENST00000680409.1:n.766T>C
ENST00000681852.1:c.298T>C ENSP00000505750.1:p.Trp100Arg
ENST00000371906.4:c.298T>C ENSP00000360973.4:p.Trp100Arg
NM_000686.4:c.298T>C NP_000677.2:p.Trp100Arg
XM_011537533.1:c.298T>C XP_011535835.1:p.Trp100Arg
NM_000686.5:c.298T>C MANE Select NP_000677.2:p.Trp100Arg
NM_001385624.1:c.298T>C NP_001372553.1:p.Trp100Arg
Search 100 bp 5'
Search 100 bp 3'