Canonical Allele Identifier: CA2366528951
Gene: CD40 HGNC NCBI

Linked Data

dbSNP Id: rs1600649956
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118244A>C , CM000682.2:g.46118244A>C GRCh38
NC_000020.10:g.44746883A>C , CM000682.1:g.44746883A>C GRCh37
NC_000020.9:g.44180290A>C NCBI36
NG_007279.1:g.4978A>C , LRG_40:g.4978A>C

Transcript Alleles

HGVS Amino-acid change
XM_005260619.3:c.-100A>C XP_005260676.1:n.-100A>C
XM_011529109.2:c.-100A>C XP_011527411.1:n.-100A>C
XM_017028135.1:c.-100A>C XP_016883624.1:n.-100A>C
XM_017028136.1:c.-100A>C XP_016883625.1:n.-100A>C
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