Canonical Allele Identifier: CA184864149

Gene: TNFRSF11B

Linked Data

• dbSNP Id: rs542840106
• gnomAD v2: 8-119944968-A-G
• gnomAD v3: 8-118932729-A-G
• gnomAD v4: 8-118932729-A-G
• MyVariant Identifiers: chr8:g.119944968A>G (hg19) ; chr8:g.118932729A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118932729A>G , CM000670.2:g.118932729A>G	GRCh38
NC_000008.10:g.119944968A>G , CM000670.1:g.119944968A>G	GRCh37
NC_000008.9:g.120014149A>G	NCBI36
NG_012202.1:g.24416T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.400+202T>C MANE Select	ENSP00000297350.4:n.400+202T>C
ENST00000297350.8:c.400+202T>C	ENSP00000297350.4:n.400+202T>C
ENST00000517352.1:c.400+202T>C	ENSP00000427924.1:n.400+202T>C
NM_002546.3:c.400+202T>C	NP_002537.3:n.400+202T>C
NM_002546.4:c.400+202T>C MANE Select	NP_002537.3:n.400+202T>C