Canonical Allele Identifier: CA338455047

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12252969A>G (hg19) ; chr1:g.12192912A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192912A>G , CM000663.2:g.12192912A>G	GRCh38
NC_000001.10:g.12252969A>G , CM000663.1:g.12252969A>G	GRCh37
NC_000001.9:g.12175556A>G	NCBI36
NG_029791.1:g.30910A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000376259.7:c.601A>G MANE Select	ENSP00000365435.3:p.Thr201Ala
ENST00000376259.6:c.601A>G	ENSP00000365435.3:p.Thr201Ala
ENST00000489921.1:n.313A>G
ENST00000492361.1:n.590A>G
NM_001066.2:c.601A>G	NP_001057.1:p.Thr201Ala
XM_011542060.1:c.601A>G	XP_011540362.1:p.Thr201Ala
XM_011542061.1:c.601A>G	XP_011540363.1:p.Thr201Ala
XM_011542062.1:c.580A>G	XP_011540364.1:p.Thr194Ala
XM_011542063.1:c.601A>G	XP_011540365.1:p.Thr201Ala
XM_011542060.2:c.601A>G	XP_011540362.1:p.Thr201Ala
XM_011542063.2:c.601A>G	XP_011540365.1:p.Thr201Ala
XM_017002211.1:c.601A>G	XP_016857700.1:p.Thr201Ala
XM_017002214.1:c.16A>G	XP_016857703.1:p.Thr6Ala
XM_017002215.1:c.16A>G	XP_016857704.1:p.Thr6Ala
NM_001066.3:c.601A>G MANE Select	NP_001057.1:p.Thr201Ala