Canonical Allele Identifier: CA744874390
Gene: CD40 HGNC NCBI

Linked Data

dbSNP Id: rs1193937246

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118243G>T , CM000682.2:g.46118243G>T GRCh38
NC_000020.10:g.44746882G>T , CM000682.1:g.44746882G>T GRCh37
NC_000020.9:g.44180289G>T NCBI36
NG_007279.1:g.4977G>T , LRG_40:g.4977G>T

Transcript Alleles

HGVS Amino-acid change
XM_005260619.3:c.-101G>T XP_005260676.1:n.-101G>T
XM_011529109.2:c.-101G>T XP_011527411.1:n.-101G>T
XM_017028135.1:c.-101G>T XP_016883624.1:n.-101G>T
XM_017028136.1:c.-101G>T XP_016883625.1:n.-101G>T