Canonical Allele Identifier: CA1814482770

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118947574C= , CM000670.2:g.118947574C=	GRCh38
NC_000008.10:g.119959813C= , CM000670.1:g.119959813C=	GRCh37
NC_000008.9:g.120028994C=	NCBI36
NG_012202.1:g.9571G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000297350.9:c.30+4218G= MANE Select	ENSP00000297350.4:n.30+4218G=
ENST00000297350.8:c.30+4218G=	ENSP00000297350.4:n.30+4218G=
ENST00000517352.1:c.30+4218G=	ENSP00000427924.1:n.30+4218G=
NM_002546.3:c.30+4218G=	NP_002537.3:n.30+4218G=
NM_002546.4:c.30+4218G= MANE Select	NP_002537.3:n.30+4218G=