Canonical Allele Identifier: CA334723682
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs919811943
gnomAD v2: X-115303773-C-A
gnomAD v3: X-116172520-C-A
gnomAD v4: X-116172520-C-A
MyVariant Identifiers: chrX:g.115303773C>A (hg19) chrX:g.116172520C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172520C>A , CM000685.2:g.116172520C>A GRCh38
NC_000023.10:g.115303773C>A , CM000685.1:g.115303773C>A GRCh37
NC_000023.9:g.115217801C>A NCBI36
NG_016326.1:g.6816C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.240C>A MANE Select ENSP00000360973.4:p.Ser80Arg
ENST00000680409.1:n.708C>A
ENST00000681852.1:c.240C>A ENSP00000505750.1:p.Ser80Arg
ENST00000371906.4:c.240C>A ENSP00000360973.4:p.Ser80Arg
NM_000686.4:c.240C>A NP_000677.2:p.Ser80Arg
XM_011537533.1:c.240C>A XP_011535835.1:p.Ser80Arg
NM_000686.5:c.240C>A MANE Select NP_000677.2:p.Ser80Arg
NM_001385624.1:c.240C>A NP_001372553.1:p.Ser80Arg
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