Canonical Allele Identifier: CA10831902

Gene: TNFRSF1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12173697T>C , CM000663.2:g.12173697T>C	GRCh38
NC_000001.10:g.12233754T>C , CM000663.1:g.12233754T>C	GRCh37
NC_000001.9:g.12156341T>C	NCBI36
NG_029791.1:g.11695T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.78+6528T>C MANE Select	ENSP00000365435.3:n.78+6528T>C
ENST00000376259.6:c.78+6528T>C	ENSP00000365435.3:n.78+6528T>C
ENST00000492361.1:n.167+6528T>C
ENST00000536782.2:c.78+6528T>C	ENSP00000440425.1:n.78+6528T>C
NM_001066.2:c.78+6528T>C	NP_001057.1:n.78+6528T>C
XM_011542060.1:c.78+6528T>C	XP_011540362.1:n.78+6528T>C
XM_011542061.1:c.78+6528T>C	XP_011540363.1:n.78+6528T>C
XM_011542063.1:c.78+6528T>C	XP_011540365.1:n.78+6528T>C
XM_011542060.2:c.78+6528T>C	XP_011540362.1:n.78+6528T>C
XM_011542063.2:c.78+6528T>C	XP_011540365.1:n.78+6528T>C
XM_017002211.1:c.78+6528T>C	XP_016857700.1:n.78+6528T>C
XM_017002214.1:c.-408+6528T>C	XP_016857703.1:n.-408+6528T>C
XM_017002215.1:c.-408+6528T>C	XP_016857704.1:n.-408+6528T>C
NM_001066.3:c.78+6528T>C MANE Select	NP_001057.1:n.78+6528T>C