Canonical Allele Identifier: CA10528077

Gene: CD40LG

Linked Data

• dbSNP Id: rs764007305
• ExAC: X:135730581 C / G
• gnomAD v2: X-135730581-C-G
• gnomAD v4: X-136648422-C-G
• MyVariant Identifiers: chrX:g.135730581C>G (hg19) ; chrX:g.136648422C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648422C>G , CM000685.2:g.136648422C>G	GRCh38
NC_000023.10:g.135730581C>G , CM000685.1:g.135730581C>G	GRCh37
NC_000023.9:g.135558247C>G	NCBI36
NG_007280.1:g.5246C>G , LRG_141:g.5246C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.156+18C>G	ENSP00000512122.1:n.156+18C>G
ENST00000695725.1:c.156+18C>G	ENSP00000512123.1:n.156+18C>G
ENST00000695726.1:n.199+18C>G
ENST00000695727.1:n.143+18C>G
ENST00000695728.1:n.143+18C>G
ENST00000370629.7:c.156+18C>G MANE Select	ENSP00000359663.2:n.156+18C>G
ENST00000370628.2:c.156+18C>G	ENSP00000359662.2:n.156+18C>G
ENST00000370629.6:c.156+18C>G	ENSP00000359663.2:n.156+18C>G
NM_000074.2:c.156+18C>G , LRG_141t1:c.156+18C>G	NP_000065.1:n.156+18C>G
NM_000074.3:c.156+18C>G MANE Select	NP_000065.1:n.156+18C>G