Canonical Allele Identifier: CA886552607

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1394490859
• gnomAD v3: 1-12192724-A-G
• gnomAD v4: 1-12192724-A-G
• MyVariant Identifiers: chr1:g.12252781A>G (hg19) ; chr1:g.12192724A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192724A>G , CM000663.2:g.12192724A>G	GRCh38
NC_000001.10:g.12252781A>G , CM000663.1:g.12252781A>G	GRCh37
NC_000001.9:g.12175368A>G	NCBI36
NG_029791.1:g.30722A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.552-139A>G MANE Select	ENSP00000365435.3:n.552-139A>G
ENST00000376259.6:c.552-139A>G	ENSP00000365435.3:n.552-139A>G
ENST00000489921.1:n.264-139A>G
ENST00000492361.1:n.541-139A>G
NM_001066.2:c.552-139A>G	NP_001057.1:n.552-139A>G
XM_011542060.1:c.552-139A>G	XP_011540362.1:n.552-139A>G
XM_011542061.1:c.552-139A>G	XP_011540363.1:n.552-139A>G
XM_011542062.1:c.531-139A>G	XP_011540364.1:n.531-139A>G
XM_011542063.1:c.552-139A>G	XP_011540365.1:n.552-139A>G
XM_011542060.2:c.552-139A>G	XP_011540362.1:n.552-139A>G
XM_011542063.2:c.552-139A>G	XP_011540365.1:n.552-139A>G
XM_017002211.1:c.552-139A>G	XP_016857700.1:n.552-139A>G
XM_017002214.1:c.-34-139A>G	XP_016857703.1:n.-34-139A>G
XM_017002215.1:c.-34-139A>G	XP_016857704.1:n.-34-139A>G
NM_001066.3:c.552-139A>G MANE Select	NP_001057.1:n.552-139A>G