Canonical Allele Identifier: CA10528146

Gene: CD40LG

Linked Data

• dbSNP Id: rs762639528
• ExAC: X:135741221 T / C
• gnomAD v2: X-135741221-T-C
• gnomAD v4: X-136659062-T-C
• MyVariant Identifiers: chrX:g.135741221T>C (hg19) ; chrX:g.136659062T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659062T>C , CM000685.2:g.136659062T>C	GRCh38
NC_000023.10:g.135741221T>C , CM000685.1:g.135741221T>C	GRCh37
NC_000023.9:g.135568887T>C	NCBI36
NG_007280.1:g.15886T>C , LRG_141:g.15886T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*51T>C	ENSP00000512122.1:n.*51T>C
ENST00000695725.1:c.180T>C	ENSP00000512123.1:p.Asp60=
ENST00000695726.1:n.2401T>C
ENST00000695729.1:n.3236T>C
ENST00000370629.7:c.433T>C MANE Select	ENSP00000359663.2:p.Tyr145His
ENST00000370628.2:c.370T>C	ENSP00000359662.2:p.Tyr124His
ENST00000370629.6:c.433T>C	ENSP00000359663.2:p.Tyr145His
NM_000074.2:c.433T>C , LRG_141t1:c.433T>C	NP_000065.1:p.Tyr145His
NM_000074.3:c.433T>C MANE Select	NP_000065.1:p.Tyr145His