Canonical Allele Identifier: CA2653131521
Gene: CD40 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118252C>A , CM000682.2:g.46118252C>A GRCh38
NC_000020.10:g.44746891C>A , CM000682.1:g.44746891C>A GRCh37
NC_000020.9:g.44180298C>A NCBI36
NG_007279.1:g.4986C>A , LRG_40:g.4986C>A

Transcript Alleles

HGVS Amino-acid change
XM_005260617.2:c.-92C>A XP_005260674.1:n.-92C>A
XM_005260619.2:c.-92C>A XP_005260676.1:n.-92C>A
XM_011529109.1:c.-92C>A XP_011527411.1:n.-92C>A
XR_936660.1:n.3C>A
XM_005260619.3:c.-92C>A XP_005260676.1:n.-92C>A
XM_011529109.2:c.-92C>A XP_011527411.1:n.-92C>A
XM_017028135.1:c.-92C>A XP_016883624.1:n.-92C>A
XM_017028136.1:c.-92C>A XP_016883625.1:n.-92C>A