Canonical Allele Identifier: CA371920390

Gene: TNFRSF11B

Linked Data

• MyVariant Identifiers: chr8:g.119945185C>T (hg19) ; chr8:g.118932946C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118932946C>T , CM000670.2:g.118932946C>T	GRCh38
NC_000008.10:g.119945185C>T , CM000670.1:g.119945185C>T	GRCh37
NC_000008.9:g.120014366C>T	NCBI36
NG_012202.1:g.24199G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.385G>A MANE Select	ENSP00000297350.4:p.Gly129Arg
ENST00000297350.8:c.385G>A	ENSP00000297350.4:p.Gly129Arg
ENST00000517352.1:c.385G>A	ENSP00000427924.1:p.Gly129Arg
NM_002546.3:c.385G>A	NP_002537.3:p.Gly129Arg
NM_002546.4:c.385G>A MANE Select	NP_002537.3:p.Gly129Arg