Canonical Allele Identifier: CA2623646065
Gene: TNFSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267210T>C , CM000675.2:g.108267210T>C GRCh38
NC_000013.10:g.108919558T>C , CM000675.1:g.108919558T>C GRCh37
NC_000013.9:g.107717559T>C NCBI36
NG_029524.1:g.2582T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2890T>C
XR_931715.1:n.1845T>C