Canonical Allele Identifier: CA2117826529
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs940778927

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267117G>T , CM000675.2:g.108267117G>T GRCh38
NC_000013.10:g.108919465G>T , CM000675.1:g.108919465G>T GRCh37
NC_000013.9:g.107717466G>T NCBI36
NG_029524.1:g.2489G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2983G>T
XR_931715.1:n.1752G>T