Canonical Allele Identifier: CA1137629971
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs2076126338

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136658934C>T , CM000685.2:g.136658934C>T GRCh38
NC_000023.10:g.135741093C>T , CM000685.1:g.135741093C>T GRCh37
NC_000023.9:g.135568759C>T NCBI36
NG_007280.1:g.15758C>T , LRG_141:g.15758C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*28-105C>T ENSP00000512122.1:n.*28-105C>T
ENST00000695725.1:c.157-105C>T ENSP00000512123.1:n.157-105C>T
ENST00000695726.1:n.2378-105C>T
ENST00000695729.1:n.3213-105C>T
ENST00000370629.7:c.410-105C>T MANE Select ENSP00000359663.2:n.410-105C>T
ENST00000370628.2:c.347-105C>T ENSP00000359662.2:n.347-105C>T
ENST00000370629.6:c.410-105C>T ENSP00000359663.2:n.410-105C>T
NM_000074.2:c.410-105C>T , LRG_141t1:c.410-105C>T NP_000065.1:n.410-105C>T
NM_000074.3:c.410-105C>T MANE Select NP_000065.1:n.410-105C>T