Canonical Allele Identifier: CA370586932

Gene: TNFRSF10B

Linked Data

• dbSNP Id: rs13265018
• MyVariant Identifiers: chr8:g.22886020A>T (hg19) ; chr8:g.23028507A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23028507A>T , CM000670.2:g.23028507A>T	GRCh38
NC_000008.10:g.22886020A>T , CM000670.1:g.22886020A>T	GRCh37
NC_000008.9:g.22941965A>T	NCBI36
NG_012145.1:g.45681T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000276431.9:c.572T>A MANE Select	ENSP00000276431.4:p.Val191Asp
ENST00000276431.8:c.572T>A	ENSP00000276431.4:p.Val191Asp
ENST00000347739.3:c.550+22T>A	ENSP00000317859.3:n.550+22T>A
ENST00000518531.5:n.322T>A
ENST00000523504.5:c.*171+22T>A	ENSP00000427999.1:n.*171+22T>A
NM_003842.4:c.572T>A	NP_003833.4:p.Val191Asp
NM_147187.2:c.550+22T>A	NP_671716.2:n.550+22T>A
NR_027140.1:n.737+22T>A
XR_949500.1:n.865T>A
NM_003842.5:c.572T>A MANE Select	NP_003833.4:p.Val191Asp
NM_147187.3:c.550+22T>A	NP_671716.2:n.550+22T>A
NR_027140.2:n.581+22T>A