Canonical Allele Identifier: CA2623646041
Gene: TNFSF13B HGNC NCBI

Linked Data

gnomAD v4: 13-108267186-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267186C>T , CM000675.2:g.108267186C>T GRCh38
NC_000013.10:g.108919534C>T , CM000675.1:g.108919534C>T GRCh37
NC_000013.9:g.107717535C>T NCBI36
NG_029524.1:g.2558C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000486502.1:n.78-2914C>T
XR_931715.1:n.1821C>T
Search 100 bp 5'
Search 100 bp 3'