Canonical Allele Identifier: CA416364714

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12252932G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192875G>T , CM000663.2:g.12192875G>T	GRCh38
NC_000001.10:g.12252932G>T , CM000663.1:g.12252932G>T	GRCh37
NC_000001.9:g.12175519G>T	NCBI36
NG_029791.1:g.30873G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.564G>T MANE Select	ENSP00000365435.3:p.Val188=
ENST00000376259.6:c.564G>T	ENSP00000365435.3:p.Val188=
ENST00000489921.1:n.276G>T
ENST00000492361.1:n.553G>T
NM_001066.2:c.564G>T	NP_001057.1:p.Val188=
XM_011542060.1:c.564G>T	XP_011540362.1:p.Val188=
XM_011542061.1:c.564G>T	XP_011540363.1:p.Val188=
XM_011542062.1:c.543G>T	XP_011540364.1:p.Val181=
XM_011542063.1:c.564G>T	XP_011540365.1:p.Val188=
XM_011542060.2:c.564G>T	XP_011540362.1:p.Val188=
XM_011542063.2:c.564G>T	XP_011540365.1:p.Val188=
XM_017002211.1:c.564G>T	XP_016857700.1:p.Val188=
XM_017002214.1:c.-22G>T	XP_016857703.1:n.-22G>T
XM_017002215.1:c.-22G>T	XP_016857704.1:n.-22G>T
NM_001066.3:c.564G>T MANE Select	NP_001057.1:p.Val188=