Canonical Allele Identifier: CA2800534207
Gene: TNFSF13B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267231T>A , CM000675.2:g.108267231T>A GRCh38
NC_000013.10:g.108919579T>A , CM000675.1:g.108919579T>A GRCh37
NC_000013.9:g.107717580T>A NCBI36
NG_029524.1:g.2603T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2869T>A
XR_931715.1:n.1866T>A
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