Canonical Allele Identifier: CA371920692
Gene: TNFRSF11B HGNC NCBI

Linked Data

COSMIC: COSM5351481 COSM5351482
MyVariant Identifiers: chr8:g.119945319C>A (hg19) chr8:g.118933080C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933080C>A , CM000670.2:g.118933080C>A GRCh38
NC_000008.10:g.119945319C>A , CM000670.1:g.119945319C>A GRCh37
NC_000008.9:g.120014500C>A NCBI36
NG_012202.1:g.24065G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.251G>T MANE Select ENSP00000297350.4:p.Ser84Ile
ENST00000297350.8:c.251G>T ENSP00000297350.4:p.Ser84Ile
ENST00000517352.1:c.251G>T ENSP00000427924.1:p.Ser84Ile
NM_002546.3:c.251G>T NP_002537.3:p.Ser84Ile
NM_002546.4:c.251G>T MANE Select NP_002537.3:p.Ser84Ile
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Search 100 bp 3'