Canonical Allele Identifier: CA1814471169

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118933080C= , CM000670.2:g.118933080C=	GRCh38
NC_000008.10:g.119945319C= , CM000670.1:g.119945319C=	GRCh37
NC_000008.9:g.120014500C=	NCBI36
NG_012202.1:g.24065G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.251G= MANE Select	ENSP00000297350.4:p.Ser84=
ENST00000297350.8:c.251G=	ENSP00000297350.4:p.Ser84=
ENST00000517352.1:c.251G=	ENSP00000427924.1:p.Ser84=
NM_002546.3:c.251G=	NP_002537.3:p.Ser84=
NM_002546.4:c.251G= MANE Select	NP_002537.3:p.Ser84=