Canonical Allele Identifier: CA2623646079
Gene: TNFSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267247del , CM000675.2:g.108267247del GRCh38
NC_000013.10:g.108919595del , CM000675.1:g.108919595del GRCh37
NC_000013.9:g.107717596del NCBI36
NG_029524.1:g.2619del

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2853del
XR_931715.1:n.1882del