Canonical Allele Identifier: CA960055306
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1880494521

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267236C>A , CM000675.2:g.108267236C>A GRCh38
NC_000013.10:g.108919584C>A , CM000675.1:g.108919584C>A GRCh37
NC_000013.9:g.107717585C>A NCBI36
NG_029524.1:g.2608C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000486502.1:n.78-2864C>A
XR_931715.1:n.1871C>A