Canonical Allele Identifier: CA2117826536
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267138T= , CM000675.2:g.108267138T= GRCh38
NC_000013.10:g.108919486T= , CM000675.1:g.108919486T= GRCh37
NC_000013.9:g.107717487T= NCBI36
NG_029524.1:g.2510T=

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2962T=
XR_931715.1:n.1773T=