Canonical Allele Identifier: CA2581156911
Gene: TNFSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267195T>G , CM000675.2:g.108267195T>G GRCh38
NC_000013.10:g.108919543T>G , CM000675.1:g.108919543T>G GRCh37
NC_000013.9:g.107717544T>G NCBI36
NG_029524.1:g.2567T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2905T>G
XR_931715.1:n.1830T>G