Canonical Allele Identifier: CA849972173

Gene: TNFRSF10B

Linked Data

• dbSNP Id: rs1389353396
• gnomAD v3: 8-23034795-G-C
• gnomAD v4: 8-23034795-G-C
• MyVariant Identifiers: chr8:g.22892308G>C (hg19) ; chr8:g.23034795G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23034795G>C , CM000670.2:g.23034795G>C	GRCh38
NC_000008.10:g.22892308G>C , CM000670.1:g.22892308G>C	GRCh37
NC_000008.9:g.22948253G>C	NCBI36
NG_012145.1:g.39393C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000276431.9:c.251-3923C>G MANE Select	ENSP00000276431.4:n.251-3923C>G
ENST00000276431.8:c.251-3923C>G	ENSP00000276431.4:n.251-3923C>G
ENST00000347739.3:c.251-3923C>G	ENSP00000317859.3:n.251-3923C>G
ENST00000519910.1:n.258-3923C>G
ENST00000523504.5:c.145-3923C>G	ENSP00000427999.1:n.145-3923C>G
NM_003842.4:c.251-3923C>G	NP_003833.4:n.251-3923C>G
NM_147187.2:c.251-3923C>G	NP_671716.2:n.251-3923C>G
NR_027140.1:n.438-3923C>G
XR_949500.1:n.544-3923C>G
NM_003842.5:c.251-3923C>G MANE Select	NP_003833.4:n.251-3923C>G
NM_147187.3:c.251-3923C>G	NP_671716.2:n.251-3923C>G
NR_027140.2:n.282-3923C>G