Canonical Allele Identifier: CA315655051

Gene: CD40

Linked Data

• dbSNP Id: rs1037125026
• gnomAD v4: 20-46129216-C-G
• MyVariant Identifiers: chr20:g.44757855C>G (hg19) ; chr20:g.46129216C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129216C>G , CM000682.2:g.46129216C>G	GRCh38
NC_000020.10:g.44757855C>G , CM000682.1:g.44757855C>G	GRCh37
NC_000020.9:g.44191262C>G	NCBI36
NG_007279.1:g.15950C>G , LRG_40:g.15950C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1093C>G	ENSP00000512096.1:n.1093C>G
ENST00000695675.1:n.2886C>G
ENST00000372285.8:c.*176C>G MANE Select	ENSP00000361359.3:n.*176C>G
ENST00000372276.7:c.*336C>G	ENSP00000361350.3:n.*336C>G
ENST00000372285.7:c.*176C>G	ENSP00000361359.3:n.*176C>G
ENST00000489304.5:n.1086C>G
ENST00000620709.4:c.*557C>G	ENSP00000484074.1:n.*557C>G
NM_001250.5:c.*176C>G	NP_001241.1:n.*176C>G
NM_001302753.1:c.*336C>G	NP_001289682.1:n.*336C>G
NM_152854.3:c.*336C>G	NP_690593.1:n.*336C>G
NR_126502.1:n.1103C>G
XM_005260617.2:c.*176C>G	XP_005260674.1:n.*176C>G
XM_005260619.2:c.*176C>G	XP_005260676.1:n.*176C>G
NM_001322421.1:c.*176C>G	NP_001309350.1:n.*176C>G
NM_001322422.1:c.*176C>G	NP_001309351.1:n.*176C>G
NM_001362758.1:c.*336C>G	NP_001349687.1:n.*336C>G
NR_136327.1:n.1006C>G
XM_005260619.3:c.*176C>G	XP_005260676.1:n.*176C>G
XM_017028135.1:c.*73C>G	XP_016883624.1:n.*73C>G
XM_017028136.1:c.*73C>G	XP_016883625.1:n.*73C>G
NM_001250.6:c.*176C>G MANE Select	NP_001241.1:n.*176C>G
NM_001302753.2:c.*336C>G	NP_001289682.1:n.*336C>G
NM_001322421.2:c.*176C>G	NP_001309350.1:n.*176C>G
NM_001322422.2:c.*176C>G	NP_001309351.1:n.*176C>G
NM_001362758.2:c.*336C>G	NP_001349687.1:n.*336C>G
NM_152854.4:c.*336C>G	NP_690593.1:n.*336C>G
NR_126502.2:n.1043C>G
NR_136327.2:n.946C>G