Canonical Allele Identifier: CA1814470950

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118932958G= , CM000670.2:g.118932958G=	GRCh38
NC_000008.10:g.119945197G= , CM000670.1:g.119945197G=	GRCh37
NC_000008.9:g.120014378G=	NCBI36
NG_012202.1:g.24187C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.373C= MANE Select	ENSP00000297350.4:p.Pro125=
ENST00000297350.8:c.373C=	ENSP00000297350.4:p.Pro125=
ENST00000517352.1:c.373C=	ENSP00000427924.1:p.Pro125=
NM_002546.3:c.373C=	NP_002537.3:p.Pro125=
NM_002546.4:c.373C= MANE Select	NP_002537.3:p.Pro125=