Canonical Allele Identifier: CA580568084

Gene: TNFRSF10B

Linked Data

• dbSNP Id: rs1451464950
• gnomAD v2: 8-22892299-A-G
• gnomAD v3: 8-23034786-A-G
• gnomAD v4: 8-23034786-A-G
• MyVariant Identifiers: chr8:g.22892299A>G (hg19) ; chr8:g.23034786A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23034786A>G , CM000670.2:g.23034786A>G	GRCh38
NC_000008.10:g.22892299A>G , CM000670.1:g.22892299A>G	GRCh37
NC_000008.9:g.22948244A>G	NCBI36
NG_012145.1:g.39402T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276431.9:c.251-3914T>C MANE Select	ENSP00000276431.4:n.251-3914T>C
ENST00000276431.8:c.251-3914T>C	ENSP00000276431.4:n.251-3914T>C
ENST00000347739.3:c.251-3914T>C	ENSP00000317859.3:n.251-3914T>C
ENST00000519910.1:n.258-3914T>C
ENST00000523504.5:c.145-3914T>C	ENSP00000427999.1:n.145-3914T>C
NM_003842.4:c.251-3914T>C	NP_003833.4:n.251-3914T>C
NM_147187.2:c.251-3914T>C	NP_671716.2:n.251-3914T>C
NR_027140.1:n.438-3914T>C
XR_949500.1:n.544-3914T>C
NM_003842.5:c.251-3914T>C MANE Select	NP_003833.4:n.251-3914T>C
NM_147187.3:c.251-3914T>C	NP_671716.2:n.251-3914T>C
NR_027140.2:n.282-3914T>C