Canonical Allele Identifier: CA2623646033
Gene: TNFSF13B HGNC NCBI

Linked Data

gnomAD v4: 13-108267176-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267176G>T , CM000675.2:g.108267176G>T GRCh38
NC_000013.10:g.108919524G>T , CM000675.1:g.108919524G>T GRCh37
NC_000013.9:g.107717525G>T NCBI36
NG_029524.1:g.2548G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2924G>T
XR_931715.1:n.1811G>T
Search 100 bp 5'
Search 100 bp 3'