Canonical Allele Identifier: CA184864173
Gene: TNFRSF11B HGNC NCBI

Linked Data

dbSNP Id: rs772995755
MyVariant Identifiers: chr8:g.119945206T>G (hg19) chr8:g.118932967T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118932967T>G , CM000670.2:g.118932967T>G GRCh38
NC_000008.10:g.119945206T>G , CM000670.1:g.119945206T>G GRCh37
NC_000008.9:g.120014387T>G NCBI36
NG_012202.1:g.24178A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.364A>C MANE Select ENSP00000297350.4:p.Arg122=
ENST00000297350.8:c.364A>C ENSP00000297350.4:p.Arg122=
ENST00000517352.1:c.364A>C ENSP00000427924.1:p.Arg122=
NM_002546.3:c.364A>C NP_002537.3:p.Arg122=
NM_002546.4:c.364A>C MANE Select NP_002537.3:p.Arg122=
Search 100 bp 5'
Search 100 bp 3'