Canonical Allele Identifier: CA1770724690

Gene: TNFRSF10B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23034679T= , CM000670.2:g.23034679T=	GRCh38
NC_000008.10:g.22892192T= , CM000670.1:g.22892192T=	GRCh37
NC_000008.9:g.22948137T=	NCBI36
NG_012145.1:g.39509A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000276431.9:c.251-3807A= MANE Select	ENSP00000276431.4:n.251-3807A=
ENST00000276431.8:c.251-3807A=	ENSP00000276431.4:n.251-3807A=
ENST00000347739.3:c.251-3807A=	ENSP00000317859.3:n.251-3807A=
ENST00000519910.1:n.258-3807A=
ENST00000523504.5:c.145-3807A=	ENSP00000427999.1:n.145-3807A=
NM_003842.4:c.251-3807A=	NP_003833.4:n.251-3807A=
NM_147187.2:c.251-3807A=	NP_671716.2:n.251-3807A=
NR_027140.1:n.438-3807A=
XR_949500.1:n.544-3807A=
NM_003842.5:c.251-3807A= MANE Select	NP_003833.4:n.251-3807A=
NM_147187.3:c.251-3807A=	NP_671716.2:n.251-3807A=
NR_027140.2:n.282-3807A=