Canonical Allele Identifier: CA521206696

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs1291955429
• gnomAD v2: 1-12262768-A-G
• gnomAD v3: 1-12202711-A-G
• gnomAD v4: 1-12202711-A-G
• MyVariant Identifiers: chr1:g.12262768A>G (hg19) ; chr1:g.12202711A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12202711A>G , CM000663.2:g.12202711A>G	GRCh38
NC_000001.10:g.12262768A>G , CM000663.1:g.12262768A>G	GRCh37
NC_000001.9:g.12185355A>G	NCBI36
NG_029791.1:g.40709A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.1105+540A>G MANE Select	ENSP00000365435.3:n.1105+540A>G
ENST00000376259.6:c.1105+540A>G	ENSP00000365435.3:n.1105+540A>G
ENST00000492361.1:n.1094+540A>G
NM_001066.2:c.1105+540A>G	NP_001057.1:n.1105+540A>G
XM_011542060.1:c.1171+139A>G	XP_011540362.1:n.1171+139A>G
XM_011542061.1:c.1171+139A>G	XP_011540363.1:n.1171+139A>G
XM_011542062.1:c.1150+139A>G	XP_011540364.1:n.1150+139A>G
XM_011542063.1:c.1105+540A>G	XP_011540365.1:n.1105+540A>G
XM_011542060.2:c.1171+139A>G	XP_011540362.1:n.1171+139A>G
XM_011542063.2:c.1105+540A>G	XP_011540365.1:n.1105+540A>G
XM_017002214.1:c.586+139A>G	XP_016857703.1:n.586+139A>G
XM_017002215.1:c.520+540A>G	XP_016857704.1:n.520+540A>G
NM_001066.3:c.1105+540A>G MANE Select	NP_001057.1:n.1105+540A>G