Canonical Allele Identifier: CA2366528952
Gene: CD40 HGNC NCBI

Linked Data

dbSNP Id: rs2085247118
gnomAD v4: 20-46118247-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118247C>A , CM000682.2:g.46118247C>A GRCh38
NC_000020.10:g.44746886C>A , CM000682.1:g.44746886C>A GRCh37
NC_000020.9:g.44180293C>A NCBI36
NG_007279.1:g.4981C>A , LRG_40:g.4981C>A

Transcript Alleles

HGVS Amino-acid change
XM_005260619.3:c.-97C>A XP_005260676.1:n.-97C>A
XM_011529109.2:c.-97C>A XP_011527411.1:n.-97C>A
XM_017028135.1:c.-97C>A XP_016883624.1:n.-97C>A
XM_017028136.1:c.-97C>A XP_016883625.1:n.-97C>A
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