Canonical Allele Identifier: CA2643342644
Gene: TNFRSF1B HGNC NCBI

Linked Data

gnomAD v4: 1-12208447-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12208447T>A , CM000663.2:g.12208447T>A GRCh38
NC_000001.10:g.12268504T>A , CM000663.1:g.12268504T>A GRCh37
NC_000001.9:g.12191091T>A NCBI36
NG_029791.1:g.46445T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376259.7:c.*1427T>A MANE Select ENSP00000365435.3:n.*1427T>A
ENST00000376259.6:c.*1427T>A ENSP00000365435.3:n.*1427T>A
ENST00000492361.1:n.2802T>A
NM_001066.2:c.*1427T>A NP_001057.1:n.*1427T>A
XM_011542060.1:c.*1427T>A XP_011540362.1:n.*1427T>A
XM_011542061.1:c.*1427T>A XP_011540363.1:n.*1427T>A
XM_011542062.1:c.2861T>A XP_011540364.1:n.2861T>A
XM_011542063.1:c.*1427T>A XP_011540365.1:n.*1427T>A
XM_011542060.2:c.*1427T>A XP_011540362.1:n.*1427T>A
XM_011542063.2:c.*1427T>A XP_011540365.1:n.*1427T>A
XM_017002214.1:c.*1427T>A XP_016857703.1:n.*1427T>A
XM_017002215.1:c.*1427T>A XP_016857704.1:n.*1427T>A
NM_001066.3:c.*1427T>A MANE Select NP_001057.1:n.*1427T>A
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