Canonical Allele Identifier: CA338455084

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12252975A>G (hg19) ; chr1:g.12192918A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192918A>G , CM000663.2:g.12192918A>G	GRCh38
NC_000001.10:g.12252975A>G , CM000663.1:g.12252975A>G	GRCh37
NC_000001.9:g.12175562A>G	NCBI36
NG_029791.1:g.30916A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.607A>G MANE Select	ENSP00000365435.3:p.Thr203Ala
ENST00000376259.6:c.607A>G	ENSP00000365435.3:p.Thr203Ala
ENST00000489921.1:n.319A>G
ENST00000492361.1:n.596A>G
NM_001066.2:c.607A>G	NP_001057.1:p.Thr203Ala
XM_011542060.1:c.607A>G	XP_011540362.1:p.Thr203Ala
XM_011542061.1:c.607A>G	XP_011540363.1:p.Thr203Ala
XM_011542062.1:c.586A>G	XP_011540364.1:p.Thr196Ala
XM_011542063.1:c.607A>G	XP_011540365.1:p.Thr203Ala
XM_011542060.2:c.607A>G	XP_011540362.1:p.Thr203Ala
XM_011542063.2:c.607A>G	XP_011540365.1:p.Thr203Ala
XM_017002211.1:c.607A>G	XP_016857700.1:p.Thr203Ala
XM_017002214.1:c.22A>G	XP_016857703.1:p.Thr8Ala
XM_017002215.1:c.22A>G	XP_016857704.1:p.Thr8Ala
NM_001066.3:c.607A>G MANE Select	NP_001057.1:p.Thr203Ala