Canonical Allele Identifier: CA960055282
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1880492985
gnomAD v3: 13-108267167-G-A
gnomAD v4: 13-108267167-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267167G>A , CM000675.2:g.108267167G>A GRCh38
NC_000013.10:g.108919515G>A , CM000675.1:g.108919515G>A GRCh37
NC_000013.9:g.107717516G>A NCBI36
NG_029524.1:g.2539G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2933G>A
XR_931715.1:n.1802G>A
Search 100 bp 5'
Search 100 bp 3'