Canonical Allele Identifier: CA2536264446
Gene: TNFRSF10B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23034698C>T , CM000670.2:g.23034698C>T GRCh38
NC_000008.10:g.22892211C>T , CM000670.1:g.22892211C>T GRCh37
NC_000008.9:g.22948156C>T NCBI36
NG_012145.1:g.39490G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000276431.9:c.251-3826G>A MANE Select ENSP00000276431.4:n.251-3826G>A
ENST00000276431.8:c.251-3826G>A ENSP00000276431.4:n.251-3826G>A
ENST00000347739.3:c.251-3826G>A ENSP00000317859.3:n.251-3826G>A
ENST00000519910.1:n.258-3826G>A
ENST00000523504.5:c.145-3826G>A ENSP00000427999.1:n.145-3826G>A
NM_003842.4:c.251-3826G>A NP_003833.4:n.251-3826G>A
NM_147187.2:c.251-3826G>A NP_671716.2:n.251-3826G>A
NR_027140.1:n.438-3826G>A
XR_949500.1:n.544-3826G>A
NM_003842.5:c.251-3826G>A MANE Select NP_003833.4:n.251-3826G>A
NM_147187.3:c.251-3826G>A NP_671716.2:n.251-3826G>A
NR_027140.2:n.282-3826G>A
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