Canonical Allele Identifier: CA15547510
Gene: TNFRSF10B HGNC NCBI

Linked Data

dbSNP Id: rs883429
gnomAD v2: 8-22886818-C-T
gnomAD v3: 8-23029305-C-T
gnomAD v4: 8-23029305-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23029305C>T , CM000670.2:g.23029305C>T GRCh38
NC_000008.10:g.22886818C>T , CM000670.1:g.22886818C>T GRCh37
NC_000008.9:g.22942763C>T NCBI36
NG_012145.1:g.44883G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000276431.9:c.476+305G>A MANE Select ENSP00000276431.4:n.476+305G>A
ENST00000276431.8:c.476+305G>A ENSP00000276431.4:n.476+305G>A
ENST00000347739.3:c.476+305G>A ENSP00000317859.3:n.476+305G>A
ENST00000518531.5:n.226+305G>A
ENST00000519910.1:n.483+305G>A
ENST00000523504.5:c.*97+305G>A ENSP00000427999.1:n.*97+305G>A
NM_003842.4:c.476+305G>A NP_003833.4:n.476+305G>A
NM_147187.2:c.476+305G>A NP_671716.2:n.476+305G>A
NR_027140.1:n.663+305G>A
XR_949500.1:n.769+305G>A
NM_003842.5:c.476+305G>A MANE Select NP_003833.4:n.476+305G>A
NM_147187.3:c.476+305G>A NP_671716.2:n.476+305G>A
NR_027140.2:n.507+305G>A