Canonical Allele Identifier: CA255749
Gene: CD40LG HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11162
ClinVar RCV Id: RCV000011912
dbSNP Id: rs104894774

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648355T>G , CM000685.2:g.136648355T>G GRCh38
NC_000023.10:g.135730514T>G , CM000685.1:g.135730514T>G GRCh37
NC_000023.9:g.135558180T>G NCBI36
NG_007280.1:g.5179T>G , LRG_141:g.5179T>G

Transcript Alleles

HGVS Amino-acid change
NM_000074.2:c.107T>G , LRG_141t1:c.107T>G NP_000065.1:p.Met36Arg
ENST00000370628.2:c.107T>G ENSP00000359662.2:p.Met36Arg
ENST00000370629.6:c.107T>G ENSP00000359663.2:p.Met36Arg