Canonical Allele Identifier: CA256829080
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs763882394

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267203C>G , CM000675.2:g.108267203C>G GRCh38
NC_000013.10:g.108919551C>G , CM000675.1:g.108919551C>G GRCh37
NC_000013.9:g.107717552C>G NCBI36
NG_029524.1:g.2575C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2897C>G
XR_931715.1:n.1838C>G