Canonical Allele Identifier: CA2366528963
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118258C= , CM000682.2:g.46118258C= GRCh38
NC_000020.10:g.44746897C= , CM000682.1:g.44746897C= GRCh37
NC_000020.9:g.44180304C= NCBI36
NG_007279.1:g.4992C= , LRG_40:g.4992C=

Transcript Alleles

HGVS Amino-acid change
NM_001250.5:c.-86C= NP_001241.1:n.-86C=
NM_001302753.1:c.-86C= NP_001289682.1:n.-86C=
NM_152854.3:c.-86C= NP_690593.1:n.-86C=
NR_126502.1:n.5C=
XM_005260617.2:c.-86C= XP_005260674.1:n.-86C=
XM_005260619.2:c.-86C= XP_005260676.1:n.-86C=
XM_011529109.1:c.-86C= XP_011527411.1:n.-86C=
XR_936660.1:n.9C=
NM_001322421.1:c.-86C= NP_001309350.1:n.-86C=
NM_001322422.1:c.-86C= NP_001309351.1:n.-86C=
NM_001362758.1:c.-86C= NP_001349687.1:n.-86C=
NR_136327.1:n.5C=
XM_005260619.3:c.-86C= XP_005260676.1:n.-86C=
XM_011529109.2:c.-86C= XP_011527411.1:n.-86C=
XM_017028135.1:c.-86C= XP_016883624.1:n.-86C=
XM_017028136.1:c.-86C= XP_016883625.1:n.-86C=