Canonical Allele Identifier: CA612329546
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1319055308
gnomAD v2: 13-108919534-C-A
gnomAD v3: 13-108267186-C-A
gnomAD v4: 13-108267186-C-A
MyVariant Identifiers: chr13:g.108919534C>A (hg19) chr13:g.108267186C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267186C>A , CM000675.2:g.108267186C>A GRCh38
NC_000013.10:g.108919534C>A , CM000675.1:g.108919534C>A GRCh37
NC_000013.9:g.107717535C>A NCBI36
NG_029524.1:g.2558C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2914C>A
XR_931715.1:n.1821C>A
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