Canonical Allele Identifier: CA334723708
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs781903172
gnomAD v4: X-116173606-C-G
MyVariant Identifiers: chrX:g.115304859C>G (hg19) chrX:g.116173606C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173606C>G , CM000685.2:g.116173606C>G GRCh38
NC_000023.10:g.115304859C>G , CM000685.1:g.115304859C>G GRCh37
NC_000023.9:g.115218887C>G NCBI36
NG_016326.1:g.7902C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*234C>G MANE Select ENSP00000360973.4:n.*234C>G
ENST00000371906.4:c.*234C>G ENSP00000360973.4:n.*234C>G
NM_000686.4:c.*234C>G NP_000677.2:n.*234C>G
XM_011537533.1:c.*234C>G XP_011535835.1:n.*234C>G
NM_000686.5:c.*234C>G MANE Select NP_000677.2:n.*234C>G
NM_001385624.1:c.*234C>G NP_001372553.1:n.*234C>G
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