Canonical Allele Identifier: CA1137626235
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs2076095378

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648474A>C , CM000685.2:g.136648474A>C GRCh38
NC_000023.10:g.135730633A>C , CM000685.1:g.135730633A>C GRCh37
NC_000023.9:g.135558299A>C NCBI36
NG_007280.1:g.5298A>C , LRG_141:g.5298A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.156+70A>C ENSP00000512122.1:n.156+70A>C
ENST00000695725.1:c.156+70A>C ENSP00000512123.1:n.156+70A>C
ENST00000695726.1:n.199+70A>C
ENST00000695727.1:n.143+70A>C
ENST00000695728.1:n.143+70A>C
ENST00000370629.7:c.156+70A>C MANE Select ENSP00000359663.2:n.156+70A>C
ENST00000370628.2:c.156+70A>C ENSP00000359662.2:n.156+70A>C
ENST00000370629.6:c.156+70A>C ENSP00000359663.2:n.156+70A>C
NM_000074.2:c.156+70A>C , LRG_141t1:c.156+70A>C NP_000065.1:n.156+70A>C
NM_000074.3:c.156+70A>C MANE Select NP_000065.1:n.156+70A>C