Canonical Allele Identifier: CA1770724694
Gene: TNFRSF10B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23034685C= , CM000670.2:g.23034685C= GRCh38
NC_000008.10:g.22892198C= , CM000670.1:g.22892198C= GRCh37
NC_000008.9:g.22948143C= NCBI36
NG_012145.1:g.39503G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000276431.9:c.251-3813G= MANE Select ENSP00000276431.4:n.251-3813G=
ENST00000276431.8:c.251-3813G= ENSP00000276431.4:n.251-3813G=
ENST00000347739.3:c.251-3813G= ENSP00000317859.3:n.251-3813G=
ENST00000519910.1:n.258-3813G=
ENST00000523504.5:c.145-3813G= ENSP00000427999.1:n.145-3813G=
NM_003842.4:c.251-3813G= NP_003833.4:n.251-3813G=
NM_147187.2:c.251-3813G= NP_671716.2:n.251-3813G=
NR_027140.1:n.438-3813G=
XR_949500.1:n.544-3813G=
NM_003842.5:c.251-3813G= MANE Select NP_003833.4:n.251-3813G=
NM_147187.3:c.251-3813G= NP_671716.2:n.251-3813G=
NR_027140.2:n.282-3813G=