Canonical Allele Identifier: CA10497352
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs782441186
ExAC: X:115304668 T / G
gnomAD v2: X-115304668-T-G
gnomAD v4: X-116173415-T-G
MyVariant Identifiers: chrX:g.115304668T>G (hg19) chrX:g.116173415T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173415T>G , CM000685.2:g.116173415T>G GRCh38
NC_000023.10:g.115304668T>G , CM000685.1:g.115304668T>G GRCh37
NC_000023.9:g.115218696T>G NCBI36
NG_016326.1:g.7711T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*43T>G MANE Select ENSP00000360973.4:n.*43T>G
ENST00000680409.1:n.1603T>G
ENST00000371906.4:c.*43T>G ENSP00000360973.4:n.*43T>G
NM_000686.4:c.*43T>G NP_000677.2:n.*43T>G
XM_011537533.1:c.*43T>G XP_011535835.1:n.*43T>G
NM_000686.5:c.*43T>G MANE Select NP_000677.2:n.*43T>G
NM_001385624.1:c.*43T>G NP_001372553.1:n.*43T>G
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