Canonical Allele Identifier: CA644630467
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs1260521642
gnomAD v2: X-135730359-C-A
gnomAD v4: X-136648200-C-A
MyVariant Identifiers: chrX:g.135730359C>A (hg19) chrX:g.136648200C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648200C>A , CM000685.2:g.136648200C>A GRCh38
NC_000023.10:g.135730359C>A , CM000685.1:g.135730359C>A GRCh37
NC_000023.9:g.135558025C>A NCBI36
NG_007280.1:g.5024C>A , LRG_141:g.5024C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.-49C>A ENSP00000512122.1:n.-49C>A
ENST00000695725.1:c.-49C>A ENSP00000512123.1:n.-49C>A
ENST00000370629.7:c.-49C>A MANE Select ENSP00000359663.2:n.-49C>A
ENST00000370629.6:c.-49C>A ENSP00000359663.2:n.-49C>A
NM_000074.2:c.-49C>A , LRG_141t1:c.-49C>A NP_000065.1:n.-49C>A
NM_000074.3:c.-49C>A MANE Select NP_000065.1:n.-49C>A
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