Canonical Allele Identifier: CA871925807
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs1460632987
MyVariant Identifiers: chrX:g.135730324A>G (hg19) chrX:g.136648165A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648165A>G , CM000685.2:g.136648165A>G GRCh38
NC_000023.10:g.135730324A>G , CM000685.1:g.135730324A>G GRCh37
NC_000023.9:g.135557990A>G NCBI36
NG_007280.1:g.4989A>G , LRG_141:g.4989A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.-84A>G ENSP00000512122.1:n.-84A>G
ENST00000370629.7:c.-84A>G MANE Select ENSP00000359663.2:n.-84A>G
NM_000074.3:c.-84A>G MANE Select NP_000065.1:n.-84A>G
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