Canonical Allele Identifier: CA1814482949

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118947988A= , CM000670.2:g.118947988A=	GRCh38
NC_000008.10:g.119960227A= , CM000670.1:g.119960227A=	GRCh37
NC_000008.9:g.120029408A=	NCBI36
NG_012202.1:g.9157T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.30+3804T= MANE Select	ENSP00000297350.4:n.30+3804T=
ENST00000297350.8:c.30+3804T=	ENSP00000297350.4:n.30+3804T=
ENST00000517352.1:c.30+3804T=	ENSP00000427924.1:n.30+3804T=
NM_002546.3:c.30+3804T=	NP_002537.3:n.30+3804T=
NM_002546.4:c.30+3804T= MANE Select	NP_002537.3:n.30+3804T=