Canonical Allele Identifier: CA2460412651
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs2076126267

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136658903T>C , CM000685.2:g.136658903T>C GRCh38
NC_000023.10:g.135741062T>C , CM000685.1:g.135741062T>C GRCh37
NC_000023.9:g.135568728T>C NCBI36
NG_007280.1:g.15727T>C , LRG_141:g.15727T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*28-136T>C ENSP00000512122.1:n.*28-136T>C
ENST00000695725.1:c.157-136T>C ENSP00000512123.1:n.157-136T>C
ENST00000695726.1:n.2378-136T>C
ENST00000695729.1:n.3213-136T>C
ENST00000370629.7:c.410-136T>C MANE Select ENSP00000359663.2:n.410-136T>C
ENST00000370628.2:c.347-136T>C ENSP00000359662.2:n.347-136T>C
ENST00000370629.6:c.410-136T>C ENSP00000359663.2:n.410-136T>C
NM_000074.2:c.410-136T>C , LRG_141t1:c.410-136T>C NP_000065.1:n.410-136T>C
NM_000074.3:c.410-136T>C MANE Select NP_000065.1:n.410-136T>C