Canonical Allele Identifier: CA694842485
Gene: TNFSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1362922670
gnomAD v3: 13-108267150-T-C
gnomAD v4: 13-108267150-T-C
MyVariant Identifiers: chr13:g.108919498T>C (hg19) chr13:g.108267150T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267150T>C , CM000675.2:g.108267150T>C GRCh38
NC_000013.10:g.108919498T>C , CM000675.1:g.108919498T>C GRCh37
NC_000013.9:g.107717499T>C NCBI36
NG_029524.1:g.2522T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2950T>C
XR_931715.1:n.1785T>C
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