Canonical Allele Identifier: CA998662208

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1639176564
• gnomAD v3: 1-12192811-CCCAG-C
• gnomAD v4: 1-12192811-CCCAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192815_12192818del , CM000663.2:g.12192815_12192818del	GRCh38
NC_000001.10:g.12252872_12252875del , CM000663.1:g.12252872_12252875del	GRCh37
NC_000001.9:g.12175459_12175462del	NCBI36
NG_029791.1:g.30813_30816del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.552-48_552-45del MANE Select	ENSP00000365435.3:n.552-48_552-45del
ENST00000376259.6:c.552-48_552-45del	ENSP00000365435.3:n.552-48_552-45del
ENST00000489921.1:n.264-48_264-45del
ENST00000492361.1:n.541-48_541-45del
NM_001066.2:c.552-48_552-45del	NP_001057.1:n.552-48_552-45del
XM_011542060.1:c.552-48_552-45del	XP_011540362.1:n.552-48_552-45del
XM_011542061.1:c.552-48_552-45del	XP_011540363.1:n.552-48_552-45del
XM_011542062.1:c.531-48_531-45del	XP_011540364.1:n.531-48_531-45del
XM_011542063.1:c.552-48_552-45del	XP_011540365.1:n.552-48_552-45del
XM_011542060.2:c.552-48_552-45del	XP_011540362.1:n.552-48_552-45del
XM_011542063.2:c.552-48_552-45del	XP_011540365.1:n.552-48_552-45del
XM_017002211.1:c.552-48_552-45del	XP_016857700.1:n.552-48_552-45del
XM_017002214.1:c.-34-48_-34-45del	XP_016857703.1:n.-34-48_-34-45del
XM_017002215.1:c.-34-48_-34-45del	XP_016857704.1:n.-34-48_-34-45del
NM_001066.3:c.552-48_552-45del MANE Select	NP_001057.1:n.552-48_552-45del