Canonical Allele Identifier: CA256829070

Gene: TNFSF13B

Linked Data

• dbSNP Id: rs938115604
• MyVariant Identifiers: chr13:g.108919440_108919448del (hg19) ; chr13:g.108267092_108267100del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108267096_108267104del , CM000675.2:g.108267096_108267104del	GRCh38
NC_000013.10:g.108919444_108919452del , CM000675.1:g.108919444_108919452del	GRCh37
NC_000013.9:g.107717445_107717453del	NCBI36
NG_029524.1:g.2468_2476del

Transcript Alleles

HGVS	Amino-acid change
ENST00000486502.1:n.78-3004_78-2996del
XR_931715.1:n.1731_1739del