Canonical Allele Identifier: CA2623646039
Gene: TNFSF13B HGNC NCBI

Linked Data

gnomAD v4: 13-108267183-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.108267183T>C , CM000675.2:g.108267183T>C GRCh38
NC_000013.10:g.108919531T>C , CM000675.1:g.108919531T>C GRCh37
NC_000013.9:g.107717532T>C NCBI36
NG_029524.1:g.2555T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000486502.1:n.78-2917T>C
XR_931715.1:n.1818T>C
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