Canonical Allele Identifier: CA2117826538
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267144A= , CM000675.2:g.108267144A= GRCh38
NC_000013.10:g.108919492A= , CM000675.1:g.108919492A= GRCh37
NC_000013.9:g.107717493A= NCBI36
NG_029524.1:g.2516A=

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2956A=
XR_931715.1:n.1779A=