Canonical Allele Identifier: CA1814472673

Gene: TNFRSF11B

Linked Data

• dbSNP Id: rs1812373802

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118934394A>G , CM000670.2:g.118934394A>G	GRCh38
NC_000008.10:g.119946633A>G , CM000670.1:g.119946633A>G	GRCh37
NC_000008.9:g.120015814A>G	NCBI36
NG_012202.1:g.22751T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.31-1094T>C MANE Select	ENSP00000297350.4:n.31-1094T>C
ENST00000297350.8:c.31-1094T>C	ENSP00000297350.4:n.31-1094T>C
ENST00000517352.1:c.31-1094T>C	ENSP00000427924.1:n.31-1094T>C
NM_002546.3:c.31-1094T>C	NP_002537.3:n.31-1094T>C
NM_002546.4:c.31-1094T>C MANE Select	NP_002537.3:n.31-1094T>C