Canonical Allele Identifier: CA2117826520
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267101A= , CM000675.2:g.108267101A= GRCh38
NC_000013.10:g.108919449A= , CM000675.1:g.108919449A= GRCh37
NC_000013.9:g.107717450A= NCBI36
NG_029524.1:g.2473A=

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2999A=
XR_931715.1:n.1736A=