Canonical Allele Identifier: CA960055251
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1594510276

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267133A>G , CM000675.2:g.108267133A>G GRCh38
NC_000013.10:g.108919481A>G , CM000675.1:g.108919481A>G GRCh37
NC_000013.9:g.107717482A>G NCBI36
NG_029524.1:g.2505A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2967A>G
XR_931715.1:n.1768A>G