Canonical Allele Identifier: CA2623646073
Gene: TNFSF13B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267232C>A , CM000675.2:g.108267232C>A GRCh38
NC_000013.10:g.108919580C>A , CM000675.1:g.108919580C>A GRCh37
NC_000013.9:g.107717581C>A NCBI36
NG_029524.1:g.2604C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2868C>A
XR_931715.1:n.1867C>A