Canonical Allele Identifier: CA694842491
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1378485434
gnomAD v4: 13-108267178-A-G
MyVariant Identifiers: chr13:g.108919526A>G (hg19) chr13:g.108267178A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267178A>G , CM000675.2:g.108267178A>G GRCh38
NC_000013.10:g.108919526A>G , CM000675.1:g.108919526A>G GRCh37
NC_000013.9:g.107717527A>G NCBI36
NG_029524.1:g.2550A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2922A>G
XR_931715.1:n.1813A>G
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