Canonical Allele Identifier: CA4854961
Gene: TNFRSF11B HGNC NCBI

Linked Data

ClinVar Variation Id: 1396908
ClinVar RCV Id: RCV001887520 RCV004041610
dbSNP Id: rs371566584
ExAC: 8:119945314 C / T
gnomAD v2: 8-119945314-C-T
gnomAD v3: 8-118933075-C-T
gnomAD v4: 8-118933075-C-T
MyVariant Identifiers: chr8:g.119945314C>T (hg19) chr8:g.118933075C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933075C>T , CM000670.2:g.118933075C>T GRCh38
NC_000008.10:g.119945314C>T , CM000670.1:g.119945314C>T GRCh37
NC_000008.9:g.120014495C>T NCBI36
NG_012202.1:g.24070G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.256G>A MANE Select ENSP00000297350.4:p.Val86Met
ENST00000297350.8:c.256G>A ENSP00000297350.4:p.Val86Met
ENST00000517352.1:c.256G>A ENSP00000427924.1:p.Val86Met
NM_002546.3:c.256G>A NP_002537.3:p.Val86Met
NM_002546.4:c.256G>A MANE Select NP_002537.3:p.Val86Met
Search 100 bp 5'
Search 100 bp 3'