Canonical Allele Identifier: CA871926194
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs1270414622

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648486A>G , CM000685.2:g.136648486A>G GRCh38
NC_000023.10:g.135730645A>G , CM000685.1:g.135730645A>G GRCh37
NC_000023.9:g.135558311A>G NCBI36
NG_007280.1:g.5310A>G , LRG_141:g.5310A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.156+82A>G ENSP00000512122.1:n.156+82A>G
ENST00000695725.1:c.156+82A>G ENSP00000512123.1:n.156+82A>G
ENST00000695726.1:n.199+82A>G
ENST00000695727.1:n.143+82A>G
ENST00000695728.1:n.143+82A>G
ENST00000370629.7:c.156+82A>G MANE Select ENSP00000359663.2:n.156+82A>G
ENST00000370628.2:c.156+82A>G ENSP00000359662.2:n.156+82A>G
ENST00000370629.6:c.156+82A>G ENSP00000359663.2:n.156+82A>G
NM_000074.2:c.156+82A>G , LRG_141t1:c.156+82A>G NP_000065.1:n.156+82A>G
NM_000074.3:c.156+82A>G MANE Select NP_000065.1:n.156+82A>G