Allele Registry

Canonical Allele Identifier: CA4673498

Gene: TNFRSF10B HGNC NCBI
TNFRSF10B-AS1 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr8:g.23068800G>A

GRCh37 chr8:g.22926313G>A

Revel Score:

ENST00000276431 (MANE Select) 0.126

ENST00000347739 0.126

Linked Data - Sequence & Population

gnomAD v2:

8:22926313 G / A

gnomAD v3:

8:23068800 G / A

gnomAD v4:

chr8-23068800-G-A

Joint Max Group AF 0.89186491 (EAS)

Genomes Max Group AF 0.88030127 (EAS)

Exomes Max Group AF 0.89104888 (EAS)

Linked Data - NCBI & NCI

dbSNP:

1129424

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)

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