Canonical Allele Identifier: CA10528058
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs764073792
ExAC: X:135730358 G / T
gnomAD v2: X-135730358-G-T
gnomAD v4: X-136648199-G-T
MyVariant Identifiers: chrX:g.135730358G>T (hg19) chrX:g.136648199G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

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