Canonical Allele Identifier: CA256829077

Gene: TNFSF13B

Linked Data

• dbSNP Id: rs1009982449
• gnomAD v3: 13-108267145-C-T
• gnomAD v4: 13-108267145-C-T
• MyVariant Identifiers: chr13:g.108919493C>T (hg19) ; chr13:g.108267145C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108267145C>T , CM000675.2:g.108267145C>T	GRCh38
NC_000013.10:g.108919493C>T , CM000675.1:g.108919493C>T	GRCh37
NC_000013.9:g.107717494C>T	NCBI36
NG_029524.1:g.2517C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000486502.1:n.78-2955C>T
XR_931715.1:n.1780C>T