Canonical Allele Identifier: CA584551515

Gene: TNFRSF11B

Linked Data

• dbSNP Id: rs1164356590
• gnomAD v2: 8-119960070-T-G
• gnomAD v3: 8-118947831-T-G
• gnomAD v4: 8-118947831-T-G
• MyVariant Identifiers: chr8:g.119960070T>G (hg19) ; chr8:g.118947831T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118947831T>G , CM000670.2:g.118947831T>G	GRCh38
NC_000008.10:g.119960070T>G , CM000670.1:g.119960070T>G	GRCh37
NC_000008.9:g.120029251T>G	NCBI36
NG_012202.1:g.9314A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.30+3961A>C MANE Select	ENSP00000297350.4:n.30+3961A>C
ENST00000297350.8:c.30+3961A>C	ENSP00000297350.4:n.30+3961A>C
ENST00000517352.1:c.30+3961A>C	ENSP00000427924.1:n.30+3961A>C
NM_002546.3:c.30+3961A>C	NP_002537.3:n.30+3961A>C
NM_002546.4:c.30+3961A>C MANE Select	NP_002537.3:n.30+3961A>C