Canonical Allele Identifier: CA2623646056
Gene: TNFSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267199G>T , CM000675.2:g.108267199G>T GRCh38
NC_000013.10:g.108919547G>T , CM000675.1:g.108919547G>T GRCh37
NC_000013.9:g.107717548G>T NCBI36
NG_029524.1:g.2571G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2901G>T
XR_931715.1:n.1834G>T