Canonical Allele Identifier: CA416364782

Gene: TNFRSF1B

Linked Data

• MyVariant Identifiers: chr1:g.12253028G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192971G>A , CM000663.2:g.12192971G>A	GRCh38
NC_000001.10:g.12253028G>A , CM000663.1:g.12253028G>A	GRCh37
NC_000001.9:g.12175615G>A	NCBI36
NG_029791.1:g.30969G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.660G>A MANE Select	ENSP00000365435.3:p.Val220=
ENST00000376259.6:c.660G>A	ENSP00000365435.3:p.Val220=
ENST00000489921.1:n.372G>A
ENST00000492361.1:n.649G>A
NM_001066.2:c.660G>A	NP_001057.1:p.Val220=
XM_011542060.1:c.660G>A	XP_011540362.1:p.Val220=
XM_011542061.1:c.660G>A	XP_011540363.1:p.Val220=
XM_011542062.1:c.639G>A	XP_011540364.1:p.Val213=
XM_011542063.1:c.660G>A	XP_011540365.1:p.Val220=
XM_011542060.2:c.660G>A	XP_011540362.1:p.Val220=
XM_011542063.2:c.660G>A	XP_011540365.1:p.Val220=
XM_017002211.1:c.660G>A	XP_016857700.1:p.Val220=
XM_017002214.1:c.75G>A	XP_016857703.1:p.Val25=
XM_017002215.1:c.75G>A	XP_016857704.1:p.Val25=
NM_001066.3:c.660G>A MANE Select	NP_001057.1:p.Val220=