Canonical Allele Identifier: CA886552658

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1295682066
• gnomAD v3: 1-12192801-GCCCAGCCAC-G
• gnomAD v4: 1-12192801-GCCCAGCCAC-G
• MyVariant Identifiers: chr1:g.12252859_12252867del (hg19) ; chr1:g.12192802_12192810del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192811_12192819del , CM000663.2:g.12192811_12192819del	GRCh38
NC_000001.10:g.12252868_12252876del , CM000663.1:g.12252868_12252876del	GRCh37
NC_000001.9:g.12175455_12175463del	NCBI36
NG_029791.1:g.30809_30817del

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.552-52_552-44del MANE Select	ENSP00000365435.3:n.552-52_552-44del
ENST00000376259.6:c.552-52_552-44del	ENSP00000365435.3:n.552-52_552-44del
ENST00000489921.1:n.264-52_264-44del
ENST00000492361.1:n.541-52_541-44del
NM_001066.2:c.552-52_552-44del	NP_001057.1:n.552-52_552-44del
XM_011542060.1:c.552-52_552-44del	XP_011540362.1:n.552-52_552-44del
XM_011542061.1:c.552-52_552-44del	XP_011540363.1:n.552-52_552-44del
XM_011542062.1:c.531-52_531-44del	XP_011540364.1:n.531-52_531-44del
XM_011542063.1:c.552-52_552-44del	XP_011540365.1:n.552-52_552-44del
XM_011542060.2:c.552-52_552-44del	XP_011540362.1:n.552-52_552-44del
XM_011542063.2:c.552-52_552-44del	XP_011540365.1:n.552-52_552-44del
XM_017002211.1:c.552-52_552-44del	XP_016857700.1:n.552-52_552-44del
XM_017002214.1:c.-34-52_-34-44del	XP_016857703.1:n.-34-52_-34-44del
XM_017002215.1:c.-34-52_-34-44del	XP_016857704.1:n.-34-52_-34-44del
NM_001066.3:c.552-52_552-44del MANE Select	NP_001057.1:n.552-52_552-44del