Canonical Allele Identifier: CA1814472659

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118934378T= , CM000670.2:g.118934378T=	GRCh38
NC_000008.10:g.119946617T= , CM000670.1:g.119946617T=	GRCh37
NC_000008.9:g.120015798T=	NCBI36
NG_012202.1:g.22767A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000297350.9:c.31-1078A= MANE Select	ENSP00000297350.4:n.31-1078A=
ENST00000297350.8:c.31-1078A=	ENSP00000297350.4:n.31-1078A=
ENST00000517352.1:c.31-1078A=	ENSP00000427924.1:n.31-1078A=
NM_002546.3:c.31-1078A=	NP_002537.3:n.31-1078A=
NM_002546.4:c.31-1078A= MANE Select	NP_002537.3:n.31-1078A=