Canonical Allele Identifier: CA2643340238

Gene: TNFRSF1B

Linked Data

• gnomAD v4: 1-12192718-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192723del , CM000663.2:g.12192723del	GRCh38
NC_000001.10:g.12252780del , CM000663.1:g.12252780del	GRCh37
NC_000001.9:g.12175367del	NCBI36
NG_029791.1:g.30721del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.552-140del MANE Select	ENSP00000365435.3:n.552-140del
ENST00000376259.6:c.552-140del	ENSP00000365435.3:n.552-140del
ENST00000489921.1:n.264-140del
ENST00000492361.1:n.541-140del
NM_001066.2:c.552-140del	NP_001057.1:n.552-140del
XM_011542060.1:c.552-140del	XP_011540362.1:n.552-140del
XM_011542061.1:c.552-140del	XP_011540363.1:n.552-140del
XM_011542062.1:c.531-140del	XP_011540364.1:n.531-140del
XM_011542063.1:c.552-140del	XP_011540365.1:n.552-140del
XM_011542060.2:c.552-140del	XP_011540362.1:n.552-140del
XM_011542063.2:c.552-140del	XP_011540365.1:n.552-140del
XM_017002211.1:c.552-140del	XP_016857700.1:n.552-140del
XM_017002214.1:c.-34-140del	XP_016857703.1:n.-34-140del
XM_017002215.1:c.-34-140del	XP_016857704.1:n.-34-140del
NM_001066.3:c.552-140del MANE Select	NP_001057.1:n.552-140del