Canonical Allele Identifier: CA2579235769

Gene: TNFRSF11B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118932896G>A , CM000670.2:g.118932896G>A	GRCh38
NC_000008.10:g.119945135G>A , CM000670.1:g.119945135G>A	GRCh37
NC_000008.9:g.120014316G>A	NCBI36
NG_012202.1:g.24249C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.400+35C>T MANE Select	ENSP00000297350.4:n.400+35C>T
ENST00000297350.8:c.400+35C>T	ENSP00000297350.4:n.400+35C>T
ENST00000517352.1:c.400+35C>T	ENSP00000427924.1:n.400+35C>T
NM_002546.3:c.400+35C>T	NP_002537.3:n.400+35C>T
NM_002546.4:c.400+35C>T MANE Select	NP_002537.3:n.400+35C>T