LDH info

Canonical Allele Identifier: CA127369
Gene: CD40 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 17749
ClinVar RCV Id: RCV000019325
dbSNP Id: rs28931586

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46122349T>C , CM000682.2:g.46122349T>C GRCh38
NC_000020.10:g.44750988T>C , CM000682.1:g.44750988T>C GRCh37
NC_000020.9:g.44184395T>C NCBI36
NG_007279.1:g.9083T>C , LRG_40:g.9083T>C

Transcript Alleles

HGVS Amino-acid change
NM_001250.5:c.247T>C VV NP_001241.1:p.Cys83Arg
NM_001302753.1:c.247T>C VV NP_001289682.1:p.Cys83Arg
NM_152854.3:c.247T>C VV NP_690593.1:p.Cys83Arg
NR_126502.1:n.337T>C
XM_005260617.2:c.247T>C XP_005260674.1:p.Cys83Arg
XM_005260619.2:c.247T>C XP_005260676.1:p.Cys83Arg
XM_011529109.1:c.247T>C XP_011527411.1:p.Cys83Arg
XR_936660.1:n.341T>C
NM_001322421.1:c.247T>C VV NP_001309350.1:p.Cys83Arg
NM_001322422.1:c.247T>C VV NP_001309351.1:p.Cys83Arg
NM_001362758.1:c.247T>C VV NP_001349687.1:p.Cys83Arg
NR_136327.1:n.337T>C
XM_005260619.3:c.247T>C XP_005260676.1:p.Cys83Arg
XM_011529109.2:c.247T>C XP_011527411.1:p.Cys83Arg
XM_017028135.1:c.247T>C XP_016883624.1:p.Cys83Arg
XM_017028136.1:c.247T>C XP_016883625.1:p.Cys83Arg
NM_001250.6:c.247T>C VV MANE Preferred NP_001241.1:p.Cys83Arg
NM_001302753.2:c.247T>C VV NP_001289682.1:p.Cys83Arg
NM_001322421.2:c.247T>C VV NP_001309350.1:p.Cys83Arg
NM_001322422.2:c.247T>C VV NP_001309351.1:p.Cys83Arg
NM_001362758.2:c.247T>C VV NP_001349687.1:p.Cys83Arg
NM_152854.4:c.247T>C VV NP_690593.1:p.Cys83Arg
NR_126502.2:n.277T>C
NR_136327.2:n.277T>C
ENST00000372276.7:c.247T>C ENSP00000361350.3:p.Cys83Arg
ENST00000372285.7:c.247T>C ENSP00000361359.3:p.Cys83Arg
ENST00000461171.1:n.32T>C
ENST00000466205.5:n.243T>C
ENST00000477696.5:n.314T>C
ENST00000489304.5:n.240T>C
ENST00000620709.4:c.247T>C ENSP00000484074.1:p.Cys83Arg