Canonical Allele Identifier: CA2366528958
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118253C= , CM000682.2:g.46118253C= GRCh38
NC_000020.10:g.44746892C= , CM000682.1:g.44746892C= GRCh37
NC_000020.9:g.44180299C= NCBI36
NG_007279.1:g.4987C= , LRG_40:g.4987C=

Transcript Alleles

HGVS Amino-acid change
XM_005260617.2:c.-91C= XP_005260674.1:n.-91C=
XM_005260619.2:c.-91C= XP_005260676.1:n.-91C=
XM_011529109.1:c.-91C= XP_011527411.1:n.-91C=
XR_936660.1:n.4C=
XM_005260619.3:c.-91C= XP_005260676.1:n.-91C=
XM_011529109.2:c.-91C= XP_011527411.1:n.-91C=
XM_017028135.1:c.-91C= XP_016883624.1:n.-91C=
XM_017028136.1:c.-91C= XP_016883625.1:n.-91C=