Canonical Allele Identifier: CA1154001382
Gene: TNFRSF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12192814A= , CM000663.2:g.12192814A= GRCh38
NC_000001.10:g.12252871A= , CM000663.1:g.12252871A= GRCh37
NC_000001.9:g.12175458A= NCBI36
NG_029791.1:g.30812A=

Transcript Alleles

HGVS Amino-acid change
ENST00000376259.7:c.552-49A= MANE Select ENSP00000365435.3:n.552-49A=
ENST00000376259.6:c.552-49A= ENSP00000365435.3:n.552-49A=
ENST00000489921.1:n.264-49A=
ENST00000492361.1:n.541-49A=
NM_001066.2:c.552-49A= NP_001057.1:n.552-49A=
XM_011542060.1:c.552-49A= XP_011540362.1:n.552-49A=
XM_011542061.1:c.552-49A= XP_011540363.1:n.552-49A=
XM_011542062.1:c.531-49A= XP_011540364.1:n.531-49A=
XM_011542063.1:c.552-49A= XP_011540365.1:n.552-49A=
XM_011542060.2:c.552-49A= XP_011540362.1:n.552-49A=
XM_011542063.2:c.552-49A= XP_011540365.1:n.552-49A=
XM_017002211.1:c.552-49A= XP_016857700.1:n.552-49A=
XM_017002214.1:c.-34-49A= XP_016857703.1:n.-34-49A=
XM_017002215.1:c.-34-49A= XP_016857704.1:n.-34-49A=
NM_001066.3:c.552-49A= MANE Select NP_001057.1:n.552-49A=