Canonical Allele Identifier: CA416364823

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12253079A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12193022A>T , CM000663.2:g.12193022A>T	GRCh38
NC_000001.10:g.12253079A>T , CM000663.1:g.12253079A>T	GRCh37
NC_000001.9:g.12175666A>T	NCBI36
NG_029791.1:g.31020A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.711A>T MANE Select	ENSP00000365435.3:p.Pro237=
ENST00000376259.6:c.711A>T	ENSP00000365435.3:p.Pro237=
ENST00000492361.1:n.700A>T
NM_001066.2:c.711A>T	NP_001057.1:p.Pro237=
XM_011542060.1:c.711A>T	XP_011540362.1:p.Pro237=
XM_011542061.1:c.711A>T	XP_011540363.1:p.Pro237=
XM_011542062.1:c.690A>T	XP_011540364.1:p.Pro230=
XM_011542063.1:c.711A>T	XP_011540365.1:p.Pro237=
XM_011542060.2:c.711A>T	XP_011540362.1:p.Pro237=
XM_011542063.2:c.711A>T	XP_011540365.1:p.Pro237=
XM_017002211.1:c.711A>T	XP_016857700.1:p.Pro237=
XM_017002214.1:c.126A>T	XP_016857703.1:p.Pro42=
XM_017002215.1:c.126A>T	XP_016857704.1:p.Pro42=
NM_001066.3:c.711A>T MANE Select	NP_001057.1:p.Pro237=