Canonical Allele Identifier: CA2623646076
Gene: TNFSF13B HGNC NCBI

Linked Data

gnomAD v4: 13-108267242-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267242G>T , CM000675.2:g.108267242G>T GRCh38
NC_000013.10:g.108919590G>T , CM000675.1:g.108919590G>T GRCh37
NC_000013.9:g.107717591G>T NCBI36
NG_029524.1:g.2614G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2858G>T
XR_931715.1:n.1877G>T
Search 100 bp 5'
Search 100 bp 3'