Canonical Allele Identifier: CA694842464

Gene: TNFSF13B

Linked Data

• dbSNP Id: rs1350795127
• MyVariant Identifiers: chr13:g.108919469G>C (hg19) ; chr13:g.108267121G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108267121G>C , CM000675.2:g.108267121G>C	GRCh38
NC_000013.10:g.108919469G>C , CM000675.1:g.108919469G>C	GRCh37
NC_000013.9:g.107717470G>C	NCBI36
NG_029524.1:g.2493G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000486502.1:n.78-2979G>C
XR_931715.1:n.1756G>C