Canonical Allele Identifier: CA2117826514
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267091_108267100delinsCATCTAAAGG , CM000675.2:g.108267091_108267100delinsCATCTAAAGG GRCh38
NC_000013.10:g.108919439_108919448delinsCATCTAAAGG , CM000675.1:g.108919439_108919448delinsCATCTAAAGG GRCh37
NC_000013.9:g.107717440_107717449delinsCATCTAAAGG NCBI36
NG_029524.1:g.2463_2472delinsCATCTAAAGG

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-3009_78-3000delinsCATCTAAAGG
XR_931715.1:n.1726_1735delinsCATCTAAAGG