Canonical Allele Identifier: CA2117826563
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267187C= , CM000675.2:g.108267187C= GRCh38
NC_000013.10:g.108919535C= , CM000675.1:g.108919535C= GRCh37
NC_000013.9:g.107717536C= NCBI36
NG_029524.1:g.2559C=

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2913C=
XR_931715.1:n.1822C=