Canonical Allele Identifier: CA2460412673
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs1752784508

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136658941A>G , CM000685.2:g.136658941A>G GRCh38
NC_000023.10:g.135741100A>G , CM000685.1:g.135741100A>G GRCh37
NC_000023.9:g.135568766A>G NCBI36
NG_007280.1:g.15765A>G , LRG_141:g.15765A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*28-98A>G ENSP00000512122.1:n.*28-98A>G
ENST00000695725.1:c.157-98A>G ENSP00000512123.1:n.157-98A>G
ENST00000695726.1:n.2378-98A>G
ENST00000695729.1:n.3213-98A>G
ENST00000370629.7:c.410-98A>G MANE Select ENSP00000359663.2:n.410-98A>G
ENST00000370628.2:c.347-98A>G ENSP00000359662.2:n.347-98A>G
ENST00000370629.6:c.410-98A>G ENSP00000359663.2:n.410-98A>G
NM_000074.2:c.410-98A>G , LRG_141t1:c.410-98A>G NP_000065.1:n.410-98A>G
NM_000074.3:c.410-98A>G MANE Select NP_000065.1:n.410-98A>G