Canonical Allele Identifier: CA2117826579
Gene: TNFSF13B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267220G= , CM000675.2:g.108267220G= GRCh38
NC_000013.10:g.108919568G= , CM000675.1:g.108919568G= GRCh37
NC_000013.9:g.107717569G= NCBI36
NG_029524.1:g.2592G=

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2880G=
XR_931715.1:n.1855G=