Canonical Allele Identifier: CA1770737887

Gene: TNFRSF10B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23043188G= , CM000670.2:g.23043188G=	GRCh38
NC_000008.10:g.22900701G= , CM000670.1:g.22900701G=	GRCh37
NC_000008.9:g.22956646G=	NCBI36
NG_012145.1:g.31000C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003842.5:c.200C= MANE Select	NP_003833.4:p.Ala67=
ENST00000276431.9:c.200C= MANE Select	ENSP00000276431.4:p.Ala67=
NM_003842.4:c.200C=	NP_003833.4:p.Ala67=
NM_147187.2:c.200C=	NP_671716.2:p.Ala67=
NM_147187.3:c.200C=	NP_671716.2:p.Ala67=
NR_027140.1:n.438-12316C=
NR_027140.2:n.282-12316C=
ENST00000276431.8:c.200C=	ENSP00000276431.4:p.Ala67=
ENST00000347739.3:c.200C=	ENSP00000317859.3:p.Ala67=
ENST00000519028.1:n.328C=
ENST00000519910.1:n.207C=
ENST00000523504.5:c.145-12316C=	ENSP00000427999.1:n.145-12316C=
XR_949500.1:n.493C=