Canonical Allele Identifier: CA371920470

Gene: TNFRSF11B

Linked Data

• MyVariant Identifiers: chr8:g.119945220A>G (hg19) ; chr8:g.118932981A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118932981A>G , CM000670.2:g.118932981A>G	GRCh38
NC_000008.10:g.119945220A>G , CM000670.1:g.119945220A>G	GRCh37
NC_000008.9:g.120014401A>G	NCBI36
NG_012202.1:g.24164T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.350T>C MANE Select	ENSP00000297350.4:p.Phe117Ser
ENST00000297350.8:c.350T>C	ENSP00000297350.4:p.Phe117Ser
ENST00000517352.1:c.350T>C	ENSP00000427924.1:p.Phe117Ser
NM_002546.3:c.350T>C	NP_002537.3:p.Phe117Ser
NM_002546.4:c.350T>C MANE Select	NP_002537.3:p.Phe117Ser