Canonical Allele Identifier: CA2643342647
Gene: TNFRSF1B HGNC NCBI

Linked Data

gnomAD v4: 1-12208449-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12208449T>C , CM000663.2:g.12208449T>C GRCh38
NC_000001.10:g.12268506T>C , CM000663.1:g.12268506T>C GRCh37
NC_000001.9:g.12191093T>C NCBI36
NG_029791.1:g.46447T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376259.7:c.*1429T>C MANE Select ENSP00000365435.3:n.*1429T>C
ENST00000376259.6:c.*1429T>C ENSP00000365435.3:n.*1429T>C
ENST00000492361.1:n.2804T>C
NM_001066.2:c.*1429T>C NP_001057.1:n.*1429T>C
XM_011542060.1:c.*1429T>C XP_011540362.1:n.*1429T>C
XM_011542061.1:c.*1429T>C XP_011540363.1:n.*1429T>C
XM_011542062.1:c.2863T>C XP_011540364.1:n.2863T>C
XM_011542063.1:c.*1429T>C XP_011540365.1:n.*1429T>C
XM_011542060.2:c.*1429T>C XP_011540362.1:n.*1429T>C
XM_011542063.2:c.*1429T>C XP_011540365.1:n.*1429T>C
XM_017002214.1:c.*1429T>C XP_016857703.1:n.*1429T>C
XM_017002215.1:c.*1429T>C XP_016857704.1:n.*1429T>C
NM_001066.3:c.*1429T>C MANE Select NP_001057.1:n.*1429T>C
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