Canonical Allele Identifier: CA2117826569
Community Standard Title: NC_000013.11:g.108267195T=
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267195T= , CM000675.2:g.108267195T= GRCh38
NC_000013.10:g.108919543T= , CM000675.1:g.108919543T= GRCh37
NC_000013.9:g.107717544T= NCBI36
NG_029524.1:g.2567T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486502.1:n.78-2905T=
XR_931715.1:n.1830T=