Canonical Allele Identifier: CA4673039
Gene: TNFRSF10B HGNC NCBI
COSMIC:
COSN168287 (not active)
MyVariant.info:
GRCh38 chr8:g.23022649G>C
GRCh37 chr8:g.22880162G>C
gnomAD v2:
8:22880162 G / C
gnomAD v3:
8:23022649 G / C
gnomAD v4:
chr8-23022649-G-C
Joint Max Group AF 0.58515003 (NFE)
Genomes Max Group AF 0.57725862 (NFE)
Exomes Max Group AF 0.58537399 (NFE)
dbSNP:
1047275
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23022649G>C , CM000670.2:g.23022649G>C GRCh38
NC_000008.10:g.22880162G>C , CM000670.1:g.22880162G>C GRCh37
NC_000008.9:g.22936107G>C NCBI36
NG_012145.1:g.51539C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000276431.9:c.*22C>G MANE Select ENSP00000276431.4:n.*22C>G
ENST00000276431.8:c.*22C>G ENSP00000276431.4:n.*22C>G
ENST00000347739.3:c.*22C>G ENSP00000317859.3:n.*22C>G
ENST00000523504.5:c.*879C>G ENSP00000427999.1:n.*879C>G
ENST00000523752.5:n.812C>G
NM_003842.4:c.*22C>G NP_003833.4:n.*22C>G
NM_147187.2:c.*22C>G NP_671716.2:n.*22C>G
NR_027140.1:n.1445C>G
XR_949500.1:n.1638C>G
NM_003842.5:c.*22C>G MANE Select NP_003833.4:n.*22C>G
NM_147187.3:c.*22C>G NP_671716.2:n.*22C>G
NR_027140.2:n.1289C>G
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