Canonical Allele Identifier: CA1814472664

Gene: TNFRSF11B

Linked Data

• dbSNP Id: rs1812373741

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118934391T>A , CM000670.2:g.118934391T>A	GRCh38
NC_000008.10:g.119946630T>A , CM000670.1:g.119946630T>A	GRCh37
NC_000008.9:g.120015811T>A	NCBI36
NG_012202.1:g.22754A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000297350.9:c.31-1091A>T MANE Select	ENSP00000297350.4:n.31-1091A>T
ENST00000297350.8:c.31-1091A>T	ENSP00000297350.4:n.31-1091A>T
ENST00000517352.1:c.31-1091A>T	ENSP00000427924.1:n.31-1091A>T
NM_002546.3:c.31-1091A>T	NP_002537.3:n.31-1091A>T
NM_002546.4:c.31-1091A>T MANE Select	NP_002537.3:n.31-1091A>T