Canonical Allele Identifier: CA2579711970
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs2148550503
gnomAD v4: X-136648196-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648196G>A , CM000685.2:g.136648196G>A GRCh38
NC_000023.10:g.135730355G>A , CM000685.1:g.135730355G>A GRCh37
NC_000023.9:g.135558021G>A NCBI36
NG_007280.1:g.5020G>A , LRG_141:g.5020G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.-53G>A ENSP00000512122.1:n.-53G>A
ENST00000695725.1:c.-53G>A ENSP00000512123.1:n.-53G>A
ENST00000370629.7:c.-53G>A MANE Select ENSP00000359663.2:n.-53G>A
ENST00000370629.6:c.-53G>A ENSP00000359663.2:n.-53G>A
NM_000074.2:c.-53G>A , LRG_141t1:c.-53G>A NP_000065.1:n.-53G>A
NM_000074.3:c.-53G>A MANE Select NP_000065.1:n.-53G>A
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