Canonical Allele Identifier: CA2117826530
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267117G= , CM000675.2:g.108267117G= GRCh38
NC_000013.10:g.108919465G= , CM000675.1:g.108919465G= GRCh37
NC_000013.9:g.107717466G= NCBI36
NG_029524.1:g.2489G=

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2983G=
XR_931715.1:n.1752G=