Canonical Allele Identifier: CA462984389
Gene: TNFRSF11B HGNC NCBI

Linked Data

gnomAD v4: 8-118933049-C-T
MyVariant Identifiers: chr8:g.119945288C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.118933049C>T , CM000670.2:g.118933049C>T GRCh38
NC_000008.10:g.119945288C>T , CM000670.1:g.119945288C>T GRCh37
NC_000008.9:g.120014469C>T NCBI36
NG_012202.1:g.24096G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297350.9:c.282G>A MANE Select ENSP00000297350.4:p.Lys94=
ENST00000297350.8:c.282G>A ENSP00000297350.4:p.Lys94=
ENST00000517352.1:c.282G>A ENSP00000427924.1:p.Lys94=
NM_002546.3:c.282G>A NP_002537.3:p.Lys94=
NM_002546.4:c.282G>A MANE Select NP_002537.3:p.Lys94=
Search 100 bp 5'
Search 100 bp 3'