Canonical Allele Identifier: CA315648798

Gene: CD40

Linked Data

• dbSNP Id: rs933310232
• gnomAD v4: 20-46118258-C-A
• MyVariant Identifiers: chr20:g.44746897C>A (hg19) ; chr20:g.46118258C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46118258C>A , CM000682.2:g.46118258C>A	GRCh38
NC_000020.10:g.44746897C>A , CM000682.1:g.44746897C>A	GRCh37
NC_000020.9:g.44180304C>A	NCBI36
NG_007279.1:g.4992C>A , LRG_40:g.4992C>A

Transcript Alleles

HGVS	Amino-acid change
NM_001250.5:c.-86C>A	NP_001241.1:n.-86C>A
NM_001302753.1:c.-86C>A	NP_001289682.1:n.-86C>A
NM_152854.3:c.-86C>A	NP_690593.1:n.-86C>A
NR_126502.1:n.5C>A
XM_005260617.2:c.-86C>A	XP_005260674.1:n.-86C>A
XM_005260619.2:c.-86C>A	XP_005260676.1:n.-86C>A
XM_011529109.1:c.-86C>A	XP_011527411.1:n.-86C>A
XR_936660.1:n.9C>A
NM_001322421.1:c.-86C>A	NP_001309350.1:n.-86C>A
NM_001322422.1:c.-86C>A	NP_001309351.1:n.-86C>A
NM_001362758.1:c.-86C>A	NP_001349687.1:n.-86C>A
NR_136327.1:n.5C>A
XM_005260619.3:c.-86C>A	XP_005260676.1:n.-86C>A
XM_011529109.2:c.-86C>A	XP_011527411.1:n.-86C>A
XM_017028135.1:c.-86C>A	XP_016883624.1:n.-86C>A
XM_017028136.1:c.-86C>A	XP_016883625.1:n.-86C>A