Canonical Allele Identifier: CA256829075
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs940778927
MyVariant Identifiers: chr13:g.108919465G>A (hg19) chr13:g.108267117G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267117G>A , CM000675.2:g.108267117G>A GRCh38
NC_000013.10:g.108919465G>A , CM000675.1:g.108919465G>A GRCh37
NC_000013.9:g.107717466G>A NCBI36
NG_029524.1:g.2489G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2983G>A
XR_931715.1:n.1752G>A
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