Canonical Allele Identifier: CA416364736

Gene: TNFRSF1B

Linked Data

• COSMIC: COSM5550993
• MyVariant Identifiers: chr1:g.12252968C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192911C>T , CM000663.2:g.12192911C>T	GRCh38
NC_000001.10:g.12252968C>T , CM000663.1:g.12252968C>T	GRCh37
NC_000001.9:g.12175555C>T	NCBI36
NG_029791.1:g.30909C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.600C>T MANE Select	ENSP00000365435.3:p.Cys200=
ENST00000376259.6:c.600C>T	ENSP00000365435.3:p.Cys200=
ENST00000489921.1:n.312C>T
ENST00000492361.1:n.589C>T
NM_001066.2:c.600C>T	NP_001057.1:p.Cys200=
XM_011542060.1:c.600C>T	XP_011540362.1:p.Cys200=
XM_011542061.1:c.600C>T	XP_011540363.1:p.Cys200=
XM_011542062.1:c.579C>T	XP_011540364.1:p.Cys193=
XM_011542063.1:c.600C>T	XP_011540365.1:p.Cys200=
XM_011542060.2:c.600C>T	XP_011540362.1:p.Cys200=
XM_011542063.2:c.600C>T	XP_011540365.1:p.Cys200=
XM_017002211.1:c.600C>T	XP_016857700.1:p.Cys200=
XM_017002214.1:c.15C>T	XP_016857703.1:p.Cys5=
XM_017002215.1:c.15C>T	XP_016857704.1:p.Cys5=
NM_001066.3:c.600C>T MANE Select	NP_001057.1:p.Cys200=