Canonical Allele Identifier: CA744874391

Gene: CD40

Linked Data

• dbSNP Id: rs1275445488
• gnomAD v4: 20-46118253-C-T
• MyVariant Identifiers: chr20:g.44746892C>T (hg19) ; chr20:g.46118253C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46118253C>T , CM000682.2:g.46118253C>T	GRCh38
NC_000020.10:g.44746892C>T , CM000682.1:g.44746892C>T	GRCh37
NC_000020.9:g.44180299C>T	NCBI36
NG_007279.1:g.4987C>T , LRG_40:g.4987C>T

Transcript Alleles

HGVS	Amino-acid change
XM_005260617.2:c.-91C>T	XP_005260674.1:n.-91C>T
XM_005260619.2:c.-91C>T	XP_005260676.1:n.-91C>T
XM_011529109.1:c.-91C>T	XP_011527411.1:n.-91C>T
XR_936660.1:n.4C>T
XM_005260619.3:c.-91C>T	XP_005260676.1:n.-91C>T
XM_011529109.2:c.-91C>T	XP_011527411.1:n.-91C>T
XM_017028135.1:c.-91C>T	XP_016883624.1:n.-91C>T
XM_017028136.1:c.-91C>T	XP_016883625.1:n.-91C>T