Canonical Allele Identifier: CA1017968133
Gene: CD40 HGNC NCBI

Linked Data

dbSNP Id: rs2085247079

Genomic Alleles

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

Transcript Alleles

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