Canonical Allele Identifier: CA338455249

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12252994T>G (hg19) ; chr1:g.12192937T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192937T>G , CM000663.2:g.12192937T>G	GRCh38
NC_000001.10:g.12252994T>G , CM000663.1:g.12252994T>G	GRCh37
NC_000001.9:g.12175581T>G	NCBI36
NG_029791.1:g.30935T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.626T>G MANE Select	ENSP00000365435.3:p.Met209Arg
ENST00000376259.6:c.626T>G	ENSP00000365435.3:p.Met209Arg
ENST00000489921.1:n.338T>G
ENST00000492361.1:n.615T>G
NM_001066.2:c.626T>G	NP_001057.1:p.Met209Arg
XM_011542060.1:c.626T>G	XP_011540362.1:p.Met209Arg
XM_011542061.1:c.626T>G	XP_011540363.1:p.Met209Arg
XM_011542062.1:c.605T>G	XP_011540364.1:p.Met202Arg
XM_011542063.1:c.626T>G	XP_011540365.1:p.Met209Arg
XM_011542060.2:c.626T>G	XP_011540362.1:p.Met209Arg
XM_011542063.2:c.626T>G	XP_011540365.1:p.Met209Arg
XM_017002211.1:c.626T>G	XP_016857700.1:p.Met209Arg
XM_017002214.1:c.41T>G	XP_016857703.1:p.Met14Arg
XM_017002215.1:c.41T>G	XP_016857704.1:p.Met14Arg
NM_001066.3:c.626T>G MANE Select	NP_001057.1:p.Met209Arg