Canonical Allele Identifier: CA2117826518
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267098_108267099delinsAG , CM000675.2:g.108267098_108267099delinsAG GRCh38
NC_000013.10:g.108919446_108919447delinsAG , CM000675.1:g.108919446_108919447delinsAG GRCh37
NC_000013.9:g.107717447_107717448delinsAG NCBI36
NG_029524.1:g.2470_2471delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-3002_78-3001delinsAG
XR_931715.1:n.1733_1734delinsAG