Canonical Allele Identifier: CA1814482793

Gene: TNFRSF11B

Linked Data

• dbSNP Id: rs1586961179

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118947620C>G , CM000670.2:g.118947620C>G	GRCh38
NC_000008.10:g.119959859C>G , CM000670.1:g.119959859C>G	GRCh37
NC_000008.9:g.120029040C>G	NCBI36
NG_012202.1:g.9525G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000297350.9:c.30+4172G>C MANE Select	ENSP00000297350.4:n.30+4172G>C
ENST00000297350.8:c.30+4172G>C	ENSP00000297350.4:n.30+4172G>C
ENST00000517352.1:c.30+4172G>C	ENSP00000427924.1:n.30+4172G>C
NM_002546.3:c.30+4172G>C	NP_002537.3:n.30+4172G>C
NM_002546.4:c.30+4172G>C MANE Select	NP_002537.3:n.30+4172G>C