Canonical Allele Identifier: CA2643340325
Gene: TNFRSF1B HGNC NCBI

Linked Data

gnomAD v4: 1-12192803-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.12192803C>A , CM000663.2:g.12192803C>A GRCh38
NC_000001.10:g.12252860C>A , CM000663.1:g.12252860C>A GRCh37
NC_000001.9:g.12175447C>A NCBI36
NG_029791.1:g.30801C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376259.7:c.552-60C>A MANE Select ENSP00000365435.3:n.552-60C>A
ENST00000376259.6:c.552-60C>A ENSP00000365435.3:n.552-60C>A
ENST00000489921.1:n.264-60C>A
ENST00000492361.1:n.541-60C>A
NM_001066.2:c.552-60C>A NP_001057.1:n.552-60C>A
XM_011542060.1:c.552-60C>A XP_011540362.1:n.552-60C>A
XM_011542061.1:c.552-60C>A XP_011540363.1:n.552-60C>A
XM_011542062.1:c.531-60C>A XP_011540364.1:n.531-60C>A
XM_011542063.1:c.552-60C>A XP_011540365.1:n.552-60C>A
XM_011542060.2:c.552-60C>A XP_011540362.1:n.552-60C>A
XM_011542063.2:c.552-60C>A XP_011540365.1:n.552-60C>A
XM_017002211.1:c.552-60C>A XP_016857700.1:n.552-60C>A
XM_017002214.1:c.-34-60C>A XP_016857703.1:n.-34-60C>A
XM_017002215.1:c.-34-60C>A XP_016857704.1:n.-34-60C>A
NM_001066.3:c.552-60C>A MANE Select NP_001057.1:n.552-60C>A