Canonical Allele Identifier: CA2117826519
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267100G= , CM000675.2:g.108267100G= GRCh38
NC_000013.10:g.108919448G= , CM000675.1:g.108919448G= GRCh37
NC_000013.9:g.107717449G= NCBI36
NG_029524.1:g.2472G=

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-3000G=
XR_931715.1:n.1735G=