Canonical Allele Identifier: CA871925809
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs1164479889
gnomAD v3: X-136648179-T-C
gnomAD v4: X-136648179-T-C
MyVariant Identifiers: chrX:g.135730338T>C (hg19) chrX:g.136648179T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648179T>C , CM000685.2:g.136648179T>C GRCh38
NC_000023.10:g.135730338T>C , CM000685.1:g.135730338T>C GRCh37
NC_000023.9:g.135558004T>C NCBI36
NG_007280.1:g.5003T>C , LRG_141:g.5003T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.-70T>C ENSP00000512122.1:n.-70T>C
ENST00000695725.1:c.-70T>C ENSP00000512123.1:n.-70T>C
ENST00000370629.7:c.-70T>C MANE Select ENSP00000359663.2:n.-70T>C
NM_000074.2:c.-70T>C , LRG_141t1:c.-70T>C NP_000065.1:n.-70T>C
NM_000074.3:c.-70T>C MANE Select NP_000065.1:n.-70T>C
Search 100 bp 5'
Search 100 bp 3'