Canonical Allele Identifier: CA2694816929
Gene: CD40LG HGNC NCBI

Linked Data

gnomAD v4: X-136648198-T-C
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Genomic Alleles

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

Transcript Alleles

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