Canonical Allele Identifier: CA694842458

Gene: TNFSF13B

Linked Data

• dbSNP Id: rs1286604837
• gnomAD v3: 13-108267116-A-G
• gnomAD v4: 13-108267116-A-G
• MyVariant Identifiers: chr13:g.108919464A>G (hg19) ; chr13:g.108267116A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108267116A>G , CM000675.2:g.108267116A>G	GRCh38
NC_000013.10:g.108919464A>G , CM000675.1:g.108919464A>G	GRCh37
NC_000013.9:g.107717465A>G	NCBI36
NG_029524.1:g.2488A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000486502.1:n.78-2984A>G
XR_931715.1:n.1751A>G