Canonical Allele Identifier: CA371920610

Gene: TNFRSF11B

Linked Data

• MyVariant Identifiers: chr8:g.119945283T>A (hg19) ; chr8:g.118933044T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.118933044T>A , CM000670.2:g.118933044T>A	GRCh38
NC_000008.10:g.119945283T>A , CM000670.1:g.119945283T>A	GRCh37
NC_000008.9:g.120014464T>A	NCBI36
NG_012202.1:g.24101A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297350.9:c.287A>T MANE Select	ENSP00000297350.4:p.Glu96Val
ENST00000297350.8:c.287A>T	ENSP00000297350.4:p.Glu96Val
ENST00000517352.1:c.287A>T	ENSP00000427924.1:p.Glu96Val
NM_002546.3:c.287A>T	NP_002537.3:p.Glu96Val
NM_002546.4:c.287A>T MANE Select	NP_002537.3:p.Glu96Val