Canonical Allele Identifier: CA960055262
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1880492594

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267146G>A , CM000675.2:g.108267146G>A GRCh38
NC_000013.10:g.108919494G>A , CM000675.1:g.108919494G>A GRCh37
NC_000013.9:g.107717495G>A NCBI36
NG_029524.1:g.2518G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2954G>A
XR_931715.1:n.1781G>A