Canonical Allele Identifier: CA2117826543
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267148_108267149delinsAT , CM000675.2:g.108267148_108267149delinsAT GRCh38
NC_000013.10:g.108919496_108919497delinsAT , CM000675.1:g.108919496_108919497delinsAT GRCh37
NC_000013.9:g.107717497_107717498delinsAT NCBI36
NG_029524.1:g.2520_2521delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2952_78-2951delinsAT
XR_931715.1:n.1783_1784delinsAT