Canonical Allele Identifier: CA4673498
Gene: TNFRSF10B HGNC NCBI
TNFRSF10B-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1129424
gnomAD v2: 8-22926313-G-A
gnomAD v3: 8-23068800-G-A
gnomAD v4: 8-23068800-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23068800G>A , CM000670.2:g.23068800G>A GRCh38
NC_000008.10:g.22926313G>A , CM000670.1:g.22926313G>A GRCh37
NC_000008.9:g.22982258G>A NCBI36
NG_012145.1:g.5388C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000276431.9:c.95C>T (TNFRSF10B) MANE Select ENSP00000276431.4:p.Pro32Leu
ENST00000276431.8:c.95C>T (TNFRSF10B) ENSP00000276431.4:p.Pro32Leu
ENST00000347739.3:c.95C>T (TNFRSF10B) ENSP00000317859.3:p.Pro32Leu
ENST00000519028.1:n.223C>T (TNFRSF10B)
ENST00000523504.5:c.95C>T (TNFRSF10B) ENSP00000427999.1:p.Pro32Leu
NM_003842.4:c.95C>T (TNFRSF10B) NP_003833.4:p.Pro32Leu
NM_147187.2:c.95C>T (TNFRSF10B) NP_671716.2:p.Pro32Leu
NR_027140.1:n.388C>T (TNFRSF10B)
NR_038873.1:n.192+380G>A (TNFRSF10B-AS1)
XR_949500.1:n.388C>T (TNFRSF10B)
NM_003842.5:c.95C>T (TNFRSF10B) MANE Select NP_003833.4:p.Pro32Leu
NM_147187.3:c.95C>T (TNFRSF10B) NP_671716.2:p.Pro32Leu
NR_027140.2:n.232C>T (TNFRSF10B)