Canonical Allele Identifier: CA2117826553

Gene: TNFSF13B

Linked Data

• dbSNP Id: rs114063620

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108267168G>A , CM000675.2:g.108267168G>A	GRCh38
NC_000013.10:g.108919516G>A , CM000675.1:g.108919516G>A	GRCh37
NC_000013.9:g.107717517G>A	NCBI36
NG_029524.1:g.2540G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000486502.1:n.78-2932G>A
XR_931715.1:n.1803G>A