Canonical Allele Identifier: CA612329547
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1306098507

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267206G>C , CM000675.2:g.108267206G>C GRCh38
NC_000013.10:g.108919554G>C , CM000675.1:g.108919554G>C GRCh37
NC_000013.9:g.107717555G>C NCBI36
NG_029524.1:g.2578G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2894G>C
XR_931715.1:n.1841G>C