Canonical Allele Identifier: CA2117826507
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267072T= , CM000675.2:g.108267072T= GRCh38
NC_000013.10:g.108919420T= , CM000675.1:g.108919420T= GRCh37
NC_000013.9:g.107717421T= NCBI36
NG_029524.1:g.2444T=

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-3028T=
XR_931715.1:n.1707T=