Canonical Allele Identifier: CA694842455

Gene: TNFSF13B

Linked Data

• dbSNP Id: rs1255166091
• gnomAD v3: 13-108267102-T-A
• gnomAD v4: 13-108267102-T-A
• MyVariant Identifiers: chr13:g.108919450T>A (hg19) ; chr13:g.108267102T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108267102T>A , CM000675.2:g.108267102T>A	GRCh38
NC_000013.10:g.108919450T>A , CM000675.1:g.108919450T>A	GRCh37
NC_000013.9:g.107717451T>A	NCBI36
NG_029524.1:g.2474T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000486502.1:n.78-2998T>A
XR_931715.1:n.1737T>A