Canonical Allele Identifier: CA1154005464

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1639420645

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12202693_12202696dup , CM000663.2:g.12202693_12202696dup	GRCh38
NC_000001.10:g.12262750_12262753dup , CM000663.1:g.12262750_12262753dup	GRCh37
NC_000001.9:g.12185337_12185340dup	NCBI36
NG_029791.1:g.40691_40694dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.1105+522_1105+525dup MANE Select	ENSP00000365435.3:n.1105+522_1105+525dup
ENST00000376259.6:c.1105+522_1105+525dup	ENSP00000365435.3:n.1105+522_1105+525dup
ENST00000492361.1:n.1094+522_1094+525dup
NM_001066.2:c.1105+522_1105+525dup	NP_001057.1:n.1105+522_1105+525dup
XM_011542060.1:c.1171+121_1171+124dup	XP_011540362.1:n.1171+121_1171+124dup
XM_011542061.1:c.1171+121_1171+124dup	XP_011540363.1:n.1171+121_1171+124dup
XM_011542062.1:c.1150+121_1150+124dup	XP_011540364.1:n.1150+121_1150+124dup
XM_011542063.1:c.1105+522_1105+525dup	XP_011540365.1:n.1105+522_1105+525dup
XM_011542060.2:c.1171+121_1171+124dup	XP_011540362.1:n.1171+121_1171+124dup
XM_011542063.2:c.1105+522_1105+525dup	XP_011540365.1:n.1105+522_1105+525dup
XM_017002214.1:c.586+121_586+124dup	XP_016857703.1:n.586+121_586+124dup
XM_017002215.1:c.520+522_520+525dup	XP_016857704.1:n.520+522_520+525dup
NM_001066.3:c.1105+522_1105+525dup MANE Select	NP_001057.1:n.1105+522_1105+525dup