Canonical Allele Identifier: CA2695436985

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs2101125724

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12202715C>T , CM000663.2:g.12202715C>T	GRCh38
NC_000001.10:g.12262772C>T , CM000663.1:g.12262772C>T	GRCh37
NC_000001.9:g.12185359C>T	NCBI36
NG_029791.1:g.40713C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.1105+544C>T MANE Select	ENSP00000365435.3:n.1105+544C>T
ENST00000376259.6:c.1105+544C>T	ENSP00000365435.3:n.1105+544C>T
ENST00000492361.1:n.1094+544C>T
NM_001066.2:c.1105+544C>T	NP_001057.1:n.1105+544C>T
XM_011542060.1:c.1171+143C>T	XP_011540362.1:n.1171+143C>T
XM_011542061.1:c.1171+143C>T	XP_011540363.1:n.1171+143C>T
XM_011542062.1:c.1150+143C>T	XP_011540364.1:n.1150+143C>T
XM_011542063.1:c.1105+544C>T	XP_011540365.1:n.1105+544C>T
XM_011542060.2:c.1171+143C>T	XP_011540362.1:n.1171+143C>T
XM_011542063.2:c.1105+544C>T	XP_011540365.1:n.1105+544C>T
XM_017002214.1:c.586+143C>T	XP_016857703.1:n.586+143C>T
XM_017002215.1:c.520+544C>T	XP_016857704.1:n.520+544C>T
NM_001066.3:c.1105+544C>T MANE Select	NP_001057.1:n.1105+544C>T