Canonical Allele Identifier: CA2604016286

Gene: TNFRSF11B

Linked Data

• dbSNP Id: rs2129926479
• gnomAD v3: 8-118947931-G-A
• gnomAD v4: 8-118947931-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118947931G>A , CM000670.2:g.118947931G>A	GRCh38
NC_000008.10:g.119960170G>A , CM000670.1:g.119960170G>A	GRCh37
NC_000008.9:g.120029351G>A	NCBI36
NG_012202.1:g.9214C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.30+3861C>T MANE Select	ENSP00000297350.4:n.30+3861C>T
ENST00000297350.8:c.30+3861C>T	ENSP00000297350.4:n.30+3861C>T
ENST00000517352.1:c.30+3861C>T	ENSP00000427924.1:n.30+3861C>T
NM_002546.3:c.30+3861C>T	NP_002537.3:n.30+3861C>T
NM_002546.4:c.30+3861C>T MANE Select	NP_002537.3:n.30+3861C>T