Canonical Allele Identifier: CA336266050
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs764073792
MyVariant Identifiers: chrX:g.136648199G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648199G>C , CM000685.2:g.136648199G>C GRCh38
NC_000023.10:g.135730358G>C , CM000685.1:g.135730358G>C GRCh37
NC_000023.9:g.135558024G>C NCBI36
NG_007280.1:g.5023G>C , LRG_141:g.5023G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.-50G>C ENSP00000512122.1:n.-50G>C
ENST00000695725.1:c.-50G>C ENSP00000512123.1:n.-50G>C
ENST00000370629.7:c.-50G>C MANE Select ENSP00000359663.2:n.-50G>C
ENST00000370629.6:c.-50G>C ENSP00000359663.2:n.-50G>C
NM_000074.2:c.-50G>C , LRG_141t1:c.-50G>C NP_000065.1:n.-50G>C
NM_000074.3:c.-50G>C MANE Select NP_000065.1:n.-50G>C