Canonical Allele Identifier: CA18037810

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs370853008
• MyVariant Identifiers: chr1:g.12268819del (hg19) ; chr1:g.12208762del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208762del , CM000663.2:g.12208762del	GRCh38
NC_000001.10:g.12268819del , CM000663.1:g.12268819del	GRCh37
NC_000001.9:g.12191406del	NCBI36
NG_029791.1:g.46760del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1742del MANE Select	ENSP00000365435.3:n.*1742del
ENST00000376259.6:c.*1742del	ENSP00000365435.3:n.*1742del
ENST00000492361.1:n.3117del
NM_001066.2:c.*1742del	NP_001057.1:n.*1742del
XM_011542060.1:c.*1742del	XP_011540362.1:n.*1742del
XM_011542061.1:c.*1742del	XP_011540363.1:n.*1742del
XM_011542062.1:c.3176del	XP_011540364.1:n.3176del
XM_011542063.1:c.*1742del	XP_011540365.1:n.*1742del
XM_011542060.2:c.*1742del	XP_011540362.1:n.*1742del
XM_011542063.2:c.*1742del	XP_011540365.1:n.*1742del
XM_017002214.1:c.*1742del	XP_016857703.1:n.*1742del
XM_017002215.1:c.*1742del	XP_016857704.1:n.*1742del
NM_001066.3:c.*1742del MANE Select	NP_001057.1:n.*1742del