Canonical Allele Identifier: CA2117826559
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267178A= , CM000675.2:g.108267178A= GRCh38
NC_000013.10:g.108919526A= , CM000675.1:g.108919526A= GRCh37
NC_000013.9:g.107717527A= NCBI36
NG_029524.1:g.2550A=

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2922A=
XR_931715.1:n.1813A=