Canonical Allele Identifier: CA694842452

Gene: TNFSF13B

Linked Data

• dbSNP Id: rs1443219366
• MyVariant Identifiers: chr13:g.108919447del (hg19) ; chr13:g.108267099del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108267100del , CM000675.2:g.108267100del	GRCh38
NC_000013.10:g.108919448del , CM000675.1:g.108919448del	GRCh37
NC_000013.9:g.107717449del	NCBI36
NG_029524.1:g.2472del

Transcript Alleles

HGVS	Amino-acid change
ENST00000486502.1:n.78-3000del
XR_931715.1:n.1735del