Canonical Allele Identifier: CA1154001391

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1331149494
• gnomAD v4: 1-12192828-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192828C>G , CM000663.2:g.12192828C>G	GRCh38
NC_000001.10:g.12252885C>G , CM000663.1:g.12252885C>G	GRCh37
NC_000001.9:g.12175472C>G	NCBI36
NG_029791.1:g.30826C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.552-35C>G MANE Select	ENSP00000365435.3:n.552-35C>G
ENST00000376259.6:c.552-35C>G	ENSP00000365435.3:n.552-35C>G
ENST00000489921.1:n.264-35C>G
ENST00000492361.1:n.541-35C>G
NM_001066.2:c.552-35C>G	NP_001057.1:n.552-35C>G
XM_011542060.1:c.552-35C>G	XP_011540362.1:n.552-35C>G
XM_011542061.1:c.552-35C>G	XP_011540363.1:n.552-35C>G
XM_011542062.1:c.531-35C>G	XP_011540364.1:n.531-35C>G
XM_011542063.1:c.552-35C>G	XP_011540365.1:n.552-35C>G
XM_011542060.2:c.552-35C>G	XP_011540362.1:n.552-35C>G
XM_011542063.2:c.552-35C>G	XP_011540365.1:n.552-35C>G
XM_017002211.1:c.552-35C>G	XP_016857700.1:n.552-35C>G
XM_017002214.1:c.-34-35C>G	XP_016857703.1:n.-34-35C>G
XM_017002215.1:c.-34-35C>G	XP_016857704.1:n.-34-35C>G
NM_001066.3:c.552-35C>G MANE Select	NP_001057.1:n.552-35C>G