Canonical Allele Identifier: CA256829073

Gene: TNFSF13B

Linked Data

• dbSNP Id: rs559491851
• MyVariant Identifiers: chr13:g.108919449A>T (hg19) ; chr13:g.108267101A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108267101A>T , CM000675.2:g.108267101A>T	GRCh38
NC_000013.10:g.108919449A>T , CM000675.1:g.108919449A>T	GRCh37
NC_000013.9:g.107717450A>T	NCBI36
NG_029524.1:g.2473A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000486502.1:n.78-2999A>T
XR_931715.1:n.1736A>T