Canonical Allele Identifier: CA371920582

Gene: TNFRSF11B

Linked Data

• MyVariant Identifiers: chr8:g.119945272T>A (hg19) ; chr8:g.118933033T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118933033T>A , CM000670.2:g.118933033T>A	GRCh38
NC_000008.10:g.119945272T>A , CM000670.1:g.119945272T>A	GRCh37
NC_000008.9:g.120014453T>A	NCBI36
NG_012202.1:g.24112A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.298A>T MANE Select	ENSP00000297350.4:p.Thr100Ser
ENST00000297350.8:c.298A>T	ENSP00000297350.4:p.Thr100Ser
ENST00000517352.1:c.298A>T	ENSP00000427924.1:p.Thr100Ser
NM_002546.3:c.298A>T	NP_002537.3:p.Thr100Ser
NM_002546.4:c.298A>T MANE Select	NP_002537.3:p.Thr100Ser