Canonical Allele Identifier: CA13871050

Gene: TNFSF13B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108290440G>C , CM000675.2:g.108290440G>C	GRCh38
NC_000013.10:g.108942788G>C , CM000675.1:g.108942788G>C	GRCh37
NC_000013.9:g.107740789G>C	NCBI36
NG_029524.1:g.25812G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375887.9:c.481+3581G>C MANE Select	ENSP00000365048.3:n.481+3581G>C
ENST00000375887.8:c.481+3581G>C	ENSP00000365048.3:n.481+3581G>C
ENST00000430559.5:c.425-12813G>C	ENSP00000389540.1:n.425-12813G>C
ENST00000479435.1:n.255+3581G>C
ENST00000542136.1:c.481+3581G>C	ENSP00000445334.1:n.481+3581G>C
NM_001145645.2:c.425-12813G>C	NP_001139117.1:n.425-12813G>C
NM_006573.4:c.481+3581G>C	NP_006564.1:n.481+3581G>C
XM_005254029.3:c.481+3581G>C	XP_005254086.1:n.481+3581G>C
XR_429277.2:n.782+1506C>G
XR_001749468.1:n.2137+3581G>C
NM_006573.5:c.481+3581G>C MANE Select	NP_006564.1:n.481+3581G>C