Canonical Allele Identifier: CA229495581
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs961717826
gnomAD v3: 11-118304689-C-T
gnomAD v4: 11-118304689-C-T
MyVariant Identifiers: chr11:g.118175404C>T (hg19) chr11:g.118304689C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118304689C>T , CM000673.2:g.118304689C>T GRCh38
NC_000011.9:g.118175404C>T , CM000673.1:g.118175404C>T GRCh37
NC_000011.8:g.117680614C>T NCBI36
NG_007383.1:g.5110C>T , LRG_38:g.5110C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000361763.8:c.-147C>T ENSP00000354566.4:n.-147C>T
NM_000733.3:c.-147C>T , LRG_38t1:c.-147C>T NP_000724.1:n.-147C>T
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