Canonical Allele Identifier: CA10528165
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs773961313
ExAC: X:135741416 A / G
gnomAD v2: X-135741416-A-G
gnomAD v3: X-136659257-A-G
gnomAD v4: X-136659257-A-G
MyVariant Identifiers: chrX:g.135741416A>G (hg19) chrX:g.136659257A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659257A>G , CM000685.2:g.136659257A>G GRCh38
NC_000023.10:g.135741416A>G , CM000685.1:g.135741416A>G GRCh37
NC_000023.9:g.135569082A>G NCBI36
NG_007280.1:g.16081A>G , LRG_141:g.16081A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*246A>G ENSP00000512122.1:n.*246A>G
ENST00000695725.1:c.*183A>G ENSP00000512123.1:n.*183A>G
ENST00000695726.1:n.2596A>G
ENST00000695729.1:n.3431A>G
ENST00000370629.7:c.628A>G MANE Select ENSP00000359663.2:p.Asn210Asp
ENST00000370628.2:c.565A>G ENSP00000359662.2:p.Asn189Asp
ENST00000370629.6:c.628A>G ENSP00000359663.2:p.Asn210Asp
NM_000074.2:c.628A>G , LRG_141t1:c.628A>G NP_000065.1:p.Asn210Asp
NM_000074.3:c.628A>G MANE Select NP_000065.1:p.Asn210Asp
Search 100 bp 5'
Search 100 bp 3'