Canonical Allele Identifier: CA1111794399

Gene: TNFRSF10B

Linked Data

• dbSNP Id: rs1672109859
• gnomAD v3: 8-23034689-GC-G
• gnomAD v4: 8-23034689-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23034690del , CM000670.2:g.23034690del	GRCh38
NC_000008.10:g.22892203del , CM000670.1:g.22892203del	GRCh37
NC_000008.9:g.22948148del	NCBI36
NG_012145.1:g.39498del

Transcript Alleles

HGVS	Amino-acid change
ENST00000276431.9:c.251-3818del MANE Select	ENSP00000276431.4:n.251-3818del
ENST00000276431.8:c.251-3818del	ENSP00000276431.4:n.251-3818del
ENST00000347739.3:c.251-3818del	ENSP00000317859.3:n.251-3818del
ENST00000519910.1:n.258-3818del
ENST00000523504.5:c.145-3818del	ENSP00000427999.1:n.145-3818del
NM_003842.4:c.251-3818del	NP_003833.4:n.251-3818del
NM_147187.2:c.251-3818del	NP_671716.2:n.251-3818del
NR_027140.1:n.438-3818del
XR_949500.1:n.544-3818del
NM_003842.5:c.251-3818del MANE Select	NP_003833.4:n.251-3818del
NM_147187.3:c.251-3818del	NP_671716.2:n.251-3818del
NR_027140.2:n.282-3818del