Canonical Allele Identifier: CA871926183

Gene: CD40LG

Linked Data

• dbSNP Id: rs1181027187
• gnomAD v3: X-136648469-T-C
• gnomAD v4: X-136648469-T-C
• MyVariant Identifiers: chrX:g.135730628T>C (hg19) ; chrX:g.136648469T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648469T>C , CM000685.2:g.136648469T>C	GRCh38
NC_000023.10:g.135730628T>C , CM000685.1:g.135730628T>C	GRCh37
NC_000023.9:g.135558294T>C	NCBI36
NG_007280.1:g.5293T>C , LRG_141:g.5293T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.156+65T>C	ENSP00000512122.1:n.156+65T>C
ENST00000695725.1:c.156+65T>C	ENSP00000512123.1:n.156+65T>C
ENST00000695726.1:n.199+65T>C
ENST00000695727.1:n.143+65T>C
ENST00000695728.1:n.143+65T>C
ENST00000370629.7:c.156+65T>C MANE Select	ENSP00000359663.2:n.156+65T>C
ENST00000370628.2:c.156+65T>C	ENSP00000359662.2:n.156+65T>C
ENST00000370629.6:c.156+65T>C	ENSP00000359663.2:n.156+65T>C
NM_000074.2:c.156+65T>C , LRG_141t1:c.156+65T>C	NP_000065.1:n.156+65T>C
NM_000074.3:c.156+65T>C MANE Select	NP_000065.1:n.156+65T>C