Canonical Allele Identifier: CA462984475
Gene: TNFRSF11B HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.119945312C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933073C>A , CM000670.2:g.118933073C>A GRCh38
NC_000008.10:g.119945312C>A , CM000670.1:g.119945312C>A GRCh37
NC_000008.9:g.120014493C>A NCBI36
NG_012202.1:g.24072G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.258G>T MANE Select ENSP00000297350.4:p.Val86=
ENST00000297350.8:c.258G>T ENSP00000297350.4:p.Val86=
ENST00000517352.1:c.258G>T ENSP00000427924.1:p.Val86=
NM_002546.3:c.258G>T NP_002537.3:p.Val86=
NM_002546.4:c.258G>T MANE Select NP_002537.3:p.Val86=
Search 100 bp 5'
Search 100 bp 3'