Canonical Allele Identifier: CA2623646068
Gene: TNFSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267222A>C , CM000675.2:g.108267222A>C GRCh38
NC_000013.10:g.108919570A>C , CM000675.1:g.108919570A>C GRCh37
NC_000013.9:g.107717571A>C NCBI36
NG_029524.1:g.2594A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2878A>C
XR_931715.1:n.1857A>C