Canonical Allele Identifier: CA2366528955
Gene: CD40 HGNC NCBI

Linked Data

dbSNP Id: rs2085247148
gnomAD v4: 20-46118248-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118248C>T , CM000682.2:g.46118248C>T GRCh38
NC_000020.10:g.44746887C>T , CM000682.1:g.44746887C>T GRCh37
NC_000020.9:g.44180294C>T NCBI36
NG_007279.1:g.4982C>T , LRG_40:g.4982C>T

Transcript Alleles

HGVS Amino-acid change
XM_005260619.3:c.-96C>T XP_005260676.1:n.-96C>T
XM_011529109.2:c.-96C>T XP_011527411.1:n.-96C>T
XM_017028135.1:c.-96C>T XP_016883624.1:n.-96C>T
XM_017028136.1:c.-96C>T XP_016883625.1:n.-96C>T
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