Canonical Allele Identifier: CA2117826584
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267239G= , CM000675.2:g.108267239G= GRCh38
NC_000013.10:g.108919587G= , CM000675.1:g.108919587G= GRCh37
NC_000013.9:g.107717588G= NCBI36
NG_029524.1:g.2611G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486502.1:n.78-2861G=
XR_931715.1:n.1874G=