Canonical Allele Identifier: CA694842469

Gene: TNFSF13B

Linked Data

• dbSNP Id: rs1245019615
• gnomAD v3: 13-108267141-C-T
• gnomAD v4: 13-108267141-C-T
• MyVariant Identifiers: chr13:g.108919489C>T (hg19) ; chr13:g.108267141C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108267141C>T , CM000675.2:g.108267141C>T	GRCh38
NC_000013.10:g.108919489C>T , CM000675.1:g.108919489C>T	GRCh37
NC_000013.9:g.107717490C>T	NCBI36
NG_029524.1:g.2513C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000486502.1:n.78-2959C>T
XR_931715.1:n.1776C>T