Canonical Allele Identifier: CA2579711962
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648172T>C , CM000685.2:g.136648172T>C GRCh38
NC_000023.10:g.135730331T>C , CM000685.1:g.135730331T>C GRCh37
NC_000023.9:g.135557997T>C NCBI36
NG_007280.1:g.4996T>C , LRG_141:g.4996T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.-77T>C ENSP00000512122.1:n.-77T>C
ENST00000370629.7:c.-77T>C MANE Select ENSP00000359663.2:n.-77T>C
NM_000074.3:c.-77T>C MANE Select NP_000065.1:n.-77T>C