Canonical Allele Identifier: CA2694816963
Gene: CD40LG HGNC NCBI

Linked Data

gnomAD v4: X-136648208-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648208A>G , CM000685.2:g.136648208A>G GRCh38
NC_000023.10:g.135730367A>G , CM000685.1:g.135730367A>G GRCh37
NC_000023.9:g.135558033A>G NCBI36
NG_007280.1:g.5032A>G , LRG_141:g.5032A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.-41A>G ENSP00000512122.1:n.-41A>G
ENST00000695725.1:c.-41A>G ENSP00000512123.1:n.-41A>G
ENST00000695726.1:n.3A>G
ENST00000370629.7:c.-41A>G MANE Select ENSP00000359663.2:n.-41A>G
ENST00000370629.6:c.-41A>G ENSP00000359663.2:n.-41A>G
NM_000074.2:c.-41A>G , LRG_141t1:c.-41A>G NP_000065.1:n.-41A>G
NM_000074.3:c.-41A>G MANE Select NP_000065.1:n.-41A>G
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