Canonical Allele Identifier: CA1154005518

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1639423779

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12202849del , CM000663.2:g.12202849del	GRCh38
NC_000001.10:g.12262906del , CM000663.1:g.12262906del	GRCh37
NC_000001.9:g.12185493del	NCBI36
NG_029791.1:g.40847del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.1105+678del MANE Select	ENSP00000365435.3:n.1105+678del
ENST00000376259.6:c.1105+678del	ENSP00000365435.3:n.1105+678del
ENST00000492361.1:n.1094+678del
NM_001066.2:c.1105+678del	NP_001057.1:n.1105+678del
XM_011542060.1:c.1171+277del	XP_011540362.1:n.1171+277del
XM_011542061.1:c.1171+277del	XP_011540363.1:n.1171+277del
XM_011542062.1:c.1150+277del	XP_011540364.1:n.1150+277del
XM_011542063.1:c.1105+678del	XP_011540365.1:n.1105+678del
XM_011542060.2:c.1171+277del	XP_011540362.1:n.1171+277del
XM_011542063.2:c.1105+678del	XP_011540365.1:n.1105+678del
XM_017002214.1:c.586+277del	XP_016857703.1:n.586+277del
XM_017002215.1:c.520+678del	XP_016857704.1:n.520+678del
NM_001066.3:c.1105+678del MANE Select	NP_001057.1:n.1105+678del