Canonical Allele Identifier: CA256829076

Gene: TNFSF13B

Linked Data

• dbSNP Id: rs1040345906
• gnomAD v3: 13-108267127-C-T
• gnomAD v4: 13-108267127-C-T
• MyVariant Identifiers: chr13:g.108919475C>T (hg19) ; chr13:g.108267127C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108267127C>T , CM000675.2:g.108267127C>T	GRCh38
NC_000013.10:g.108919475C>T , CM000675.1:g.108919475C>T	GRCh37
NC_000013.9:g.107717476C>T	NCBI36
NG_029524.1:g.2499C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000486502.1:n.78-2973C>T
XR_931715.1:n.1762C>T