Canonical Allele Identifier: CA255747
Gene: CD40LG HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11160
ClinVar RCV Id: RCV000011910
dbSNP Id: rs104894769

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659093T>C , CM000685.2:g.136659093T>C GRCh38
NC_000023.9:g.135568918T>C NCBI36
NC_000023.10:g.135741252T>C , CM000685.1:g.135741252T>C GRCh37
NG_007280.1:g.15917T>C , LRG_141:g.15917T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000370628.2:c.401T>C ENSP00000359662.2:p.Leu134Pro
ENST00000370629.6:c.464T>C ENSP00000359663.2:p.Leu155Pro
NM_000074.2:c.464T>C , LRG_141t1:c.464T>C NP_000065.1:p.Leu155Pro