Canonical Allele Identifier: CA18031424

Gene: TNFRSF1B

Linked Data

• dbSNP Id: rs551572367
• MyVariant Identifiers: chr1:g.12262762A>G (hg19) ; chr1:g.12202705A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12202705A>G , CM000663.2:g.12202705A>G	GRCh38
NC_000001.10:g.12262762A>G , CM000663.1:g.12262762A>G	GRCh37
NC_000001.9:g.12185349A>G	NCBI36
NG_029791.1:g.40703A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.1105+534A>G MANE Select	ENSP00000365435.3:n.1105+534A>G
ENST00000376259.6:c.1105+534A>G	ENSP00000365435.3:n.1105+534A>G
ENST00000492361.1:n.1094+534A>G
NM_001066.2:c.1105+534A>G	NP_001057.1:n.1105+534A>G
XM_011542060.1:c.1171+133A>G	XP_011540362.1:n.1171+133A>G
XM_011542061.1:c.1171+133A>G	XP_011540363.1:n.1171+133A>G
XM_011542062.1:c.1150+133A>G	XP_011540364.1:n.1150+133A>G
XM_011542063.1:c.1105+534A>G	XP_011540365.1:n.1105+534A>G
XM_011542060.2:c.1171+133A>G	XP_011540362.1:n.1171+133A>G
XM_011542063.2:c.1105+534A>G	XP_011540365.1:n.1105+534A>G
XM_017002214.1:c.586+133A>G	XP_016857703.1:n.586+133A>G
XM_017002215.1:c.520+534A>G	XP_016857704.1:n.520+534A>G
NM_001066.3:c.1105+534A>G MANE Select	NP_001057.1:n.1105+534A>G