Canonical Allele Identifier: CA2623646057
Gene: TNFSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267200G>A , CM000675.2:g.108267200G>A GRCh38
NC_000013.10:g.108919548G>A , CM000675.1:g.108919548G>A GRCh37
NC_000013.9:g.107717549G>A NCBI36
NG_029524.1:g.2572G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2900G>A
XR_931715.1:n.1835G>A