Canonical Allele Identifier: CA644630468
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs1477244811
gnomAD v2: X-135730365-C-T
gnomAD v4: X-136648206-C-T
MyVariant Identifiers: chrX:g.135730365C>T (hg19) chrX:g.136648206C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648206C>T , CM000685.2:g.136648206C>T GRCh38
NC_000023.10:g.135730365C>T , CM000685.1:g.135730365C>T GRCh37
NC_000023.9:g.135558031C>T NCBI36
NG_007280.1:g.5030C>T , LRG_141:g.5030C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.-43C>T ENSP00000512122.1:n.-43C>T
ENST00000695725.1:c.-43C>T ENSP00000512123.1:n.-43C>T
ENST00000695726.1:n.1C>T
ENST00000370629.7:c.-43C>T MANE Select ENSP00000359663.2:n.-43C>T
ENST00000370629.6:c.-43C>T ENSP00000359663.2:n.-43C>T
NM_000074.2:c.-43C>T , LRG_141t1:c.-43C>T NP_000065.1:n.-43C>T
NM_000074.3:c.-43C>T MANE Select NP_000065.1:n.-43C>T
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