Canonical Allele Identifier: CA338455754
Gene: TNFRSF1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12192990A>G , CM000663.2:g.12192990A>G GRCh38
NC_000001.10:g.12253047A>G , CM000663.1:g.12253047A>G GRCh37
NC_000001.9:g.12175634A>G NCBI36
NG_029791.1:g.30988A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376259.7:c.679A>G MANE Select ENSP00000365435.3:p.Thr227Ala
ENST00000376259.6:c.679A>G ENSP00000365435.3:p.Thr227Ala
ENST00000489921.1:n.391A>G
ENST00000492361.1:n.668A>G
NM_001066.2:c.679A>G NP_001057.1:p.Thr227Ala
XM_011542060.1:c.679A>G XP_011540362.1:p.Thr227Ala
XM_011542061.1:c.679A>G XP_011540363.1:p.Thr227Ala
XM_011542062.1:c.658A>G XP_011540364.1:p.Thr220Ala
XM_011542063.1:c.679A>G XP_011540365.1:p.Thr227Ala
XM_011542060.2:c.679A>G XP_011540362.1:p.Thr227Ala
XM_011542063.2:c.679A>G XP_011540365.1:p.Thr227Ala
XM_017002211.1:c.679A>G XP_016857700.1:p.Thr227Ala
XM_017002214.1:c.94A>G XP_016857703.1:p.Thr32Ala
XM_017002215.1:c.94A>G XP_016857704.1:p.Thr32Ala
NM_001066.3:c.679A>G MANE Select NP_001057.1:p.Thr227Ala