Canonical Allele Identifier: CA871925819
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs1444953302
gnomAD v3: X-136648201-C-T
gnomAD v4: X-136648201-C-T
MyVariant Identifiers: chrX:g.135730360C>T (hg19) chrX:g.136648201C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648201C>T , CM000685.2:g.136648201C>T GRCh38
NC_000023.10:g.135730360C>T , CM000685.1:g.135730360C>T GRCh37
NC_000023.9:g.135558026C>T NCBI36
NG_007280.1:g.5025C>T , LRG_141:g.5025C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.-48C>T ENSP00000512122.1:n.-48C>T
ENST00000695725.1:c.-48C>T ENSP00000512123.1:n.-48C>T
ENST00000370629.7:c.-48C>T MANE Select ENSP00000359663.2:n.-48C>T
ENST00000370629.6:c.-48C>T ENSP00000359663.2:n.-48C>T
NM_000074.2:c.-48C>T , LRG_141t1:c.-48C>T NP_000065.1:n.-48C>T
NM_000074.3:c.-48C>T MANE Select NP_000065.1:n.-48C>T
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