Canonical Allele Identifier: CA371920699

Gene: TNFRSF11B

Linked Data

• MyVariant Identifiers: chr8:g.119945322C>G (hg19) ; chr8:g.118933083C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118933083C>G , CM000670.2:g.118933083C>G	GRCh38
NC_000008.10:g.119945322C>G , CM000670.1:g.119945322C>G	GRCh37
NC_000008.9:g.120014503C>G	NCBI36
NG_012202.1:g.24062G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.248G>C MANE Select	ENSP00000297350.4:p.Cys83Ser
ENST00000297350.8:c.248G>C	ENSP00000297350.4:p.Cys83Ser
ENST00000517352.1:c.248G>C	ENSP00000427924.1:p.Cys83Ser
NM_002546.3:c.248G>C	NP_002537.3:p.Cys83Ser
NM_002546.4:c.248G>C MANE Select	NP_002537.3:p.Cys83Ser