Canonical Allele Identifier: CA1814470867

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118932906A= , CM000670.2:g.118932906A=	GRCh38
NC_000008.10:g.119945145A= , CM000670.1:g.119945145A=	GRCh37
NC_000008.9:g.120014326A=	NCBI36
NG_012202.1:g.24239T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.400+25T= MANE Select	ENSP00000297350.4:n.400+25T=
ENST00000297350.8:c.400+25T=	ENSP00000297350.4:n.400+25T=
ENST00000517352.1:c.400+25T=	ENSP00000427924.1:n.400+25T=
NM_002546.3:c.400+25T=	NP_002537.3:n.400+25T=
NM_002546.4:c.400+25T= MANE Select	NP_002537.3:n.400+25T=