Canonical Allele Identifier: CA336266049
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs200407982

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648185A>G , CM000685.2:g.136648185A>G GRCh38
NC_000023.10:g.135730344A>G , CM000685.1:g.135730344A>G GRCh37
NC_000023.9:g.135558010A>G NCBI36
NG_007280.1:g.5009A>G , LRG_141:g.5009A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.-64A>G ENSP00000512122.1:n.-64A>G
ENST00000695725.1:c.-64A>G ENSP00000512123.1:n.-64A>G
ENST00000370629.7:c.-64A>G MANE Select ENSP00000359663.2:n.-64A>G
NM_000074.2:c.-64A>G , LRG_141t1:c.-64A>G NP_000065.1:n.-64A>G
NM_000074.3:c.-64A>G MANE Select NP_000065.1:n.-64A>G