Canonical Allele Identifier: CA336267377
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs6635310
MyVariant Identifiers: chrX:g.135741107G>A (hg19) chrX:g.136658948G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136658948G>A , CM000685.2:g.136658948G>A GRCh38
NC_000023.10:g.135741107G>A , CM000685.1:g.135741107G>A GRCh37
NC_000023.9:g.135568773G>A NCBI36
NG_007280.1:g.15772G>A , LRG_141:g.15772G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*28-91G>A ENSP00000512122.1:n.*28-91G>A
ENST00000695725.1:c.157-91G>A ENSP00000512123.1:n.157-91G>A
ENST00000695726.1:n.2378-91G>A
ENST00000695729.1:n.3213-91G>A
ENST00000370629.7:c.410-91G>A MANE Select ENSP00000359663.2:n.410-91G>A
ENST00000370628.2:c.347-91G>A ENSP00000359662.2:n.347-91G>A
ENST00000370629.6:c.410-91G>A ENSP00000359663.2:n.410-91G>A
NM_000074.2:c.410-91G>A , LRG_141t1:c.410-91G>A NP_000065.1:n.410-91G>A
NM_000074.3:c.410-91G>A MANE Select NP_000065.1:n.410-91G>A
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