Canonical Allele Identifier: CA1770700870

Gene: TNFRSF10B

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23022649G>A , CM000670.2:g.23022649G>A	GRCh38
NC_000008.10:g.22880162G>A , CM000670.1:g.22880162G>A	GRCh37
NC_000008.9:g.22936107G>A	NCBI36
NG_012145.1:g.51539C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276431.9:c.*22C>T MANE Select	ENSP00000276431.4:n.*22C>T
ENST00000276431.8:c.*22C>T	ENSP00000276431.4:n.*22C>T
ENST00000347739.3:c.*22C>T	ENSP00000317859.3:n.*22C>T
ENST00000523504.5:c.*879C>T	ENSP00000427999.1:n.*879C>T
ENST00000523752.5:n.812C>T
NM_003842.4:c.*22C>T	NP_003833.4:n.*22C>T
NM_147187.2:c.*22C>T	NP_671716.2:n.*22C>T
NR_027140.1:n.1445C>T
XR_949500.1:n.1638C>T
NM_003842.5:c.*22C>T MANE Select	NP_003833.4:n.*22C>T
NM_147187.3:c.*22C>T	NP_671716.2:n.*22C>T
NR_027140.2:n.1289C>T