Canonical Allele Identifier: CA2460409127
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs2076094545
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648198T>A , CM000685.2:g.136648198T>A GRCh38
NC_000023.10:g.135730357T>A , CM000685.1:g.135730357T>A GRCh37
NC_000023.9:g.135558023T>A NCBI36
NG_007280.1:g.5022T>A , LRG_141:g.5022T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.-51T>A ENSP00000512122.1:n.-51T>A
ENST00000695725.1:c.-51T>A ENSP00000512123.1:n.-51T>A
ENST00000370629.7:c.-51T>A MANE Select ENSP00000359663.2:n.-51T>A
ENST00000370629.6:c.-51T>A ENSP00000359663.2:n.-51T>A
NM_000074.2:c.-51T>A , LRG_141t1:c.-51T>A NP_000065.1:n.-51T>A
NM_000074.3:c.-51T>A MANE Select NP_000065.1:n.-51T>A
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