Canonical Allele Identifier: CA1111794402

Gene: TNFRSF10B

Linked Data

• dbSNP Id: rs1811980035
• gnomAD v3: 8-23034696-A-AGGGT
• gnomAD v4: 8-23034696-A-AGGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23034697_23034698insGGTG , CM000670.2:g.23034697_23034698insGGTG	GRCh38
NC_000008.10:g.22892210_22892211insGGTG , CM000670.1:g.22892210_22892211insGGTG	GRCh37
NC_000008.9:g.22948155_22948156insGGTG	NCBI36
NG_012145.1:g.39491_39492insACCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000276431.9:c.251-3825_251-3824insACCC MANE Select	ENSP00000276431.4:n.251-3825_251-3824insACCC
ENST00000276431.8:c.251-3825_251-3824insACCC	ENSP00000276431.4:n.251-3825_251-3824insACCC
ENST00000347739.3:c.251-3825_251-3824insACCC	ENSP00000317859.3:n.251-3825_251-3824insACCC
ENST00000519910.1:n.258-3825_258-3824insACCC
ENST00000523504.5:c.145-3825_145-3824insACCC	ENSP00000427999.1:n.145-3825_145-3824insACCC
NM_003842.4:c.251-3825_251-3824insACCC	NP_003833.4:n.251-3825_251-3824insACCC
NM_147187.2:c.251-3825_251-3824insACCC	NP_671716.2:n.251-3825_251-3824insACCC
NR_027140.1:n.438-3825_438-3824insACCC
XR_949500.1:n.544-3825_544-3824insACCC
NM_003842.5:c.251-3825_251-3824insACCC MANE Select	NP_003833.4:n.251-3825_251-3824insACCC
NM_147187.3:c.251-3825_251-3824insACCC	NP_671716.2:n.251-3825_251-3824insACCC
NR_027140.2:n.282-3825_282-3824insACCC