Canonical Allele Identifier: CA477082575
Gene: CD3E HGNC NCBI

Linked Data

ClinVar Variation Id: 2017358
ClinVar RCV Id: RCV002835165
MyVariant Identifiers: chr11:g.118183463T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312748T>C , CM000673.2:g.118312748T>C GRCh38
NC_000011.9:g.118183463T>C , CM000673.1:g.118183463T>C GRCh37
NC_000011.8:g.117688673T>C NCBI36
NG_007383.1:g.13169T>C , LRG_38:g.13169T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.234T>C MANE Select ENSP00000354566.4:p.Asp78=
ENST00000361763.8:c.234T>C ENSP00000354566.4:p.Asp78=
ENST00000526146.5:n.780T>C
ENST00000528435.5:n.787T>C
ENST00000528600.1:c.216T>C ENSP00000433975.1:p.Asp72=
ENST00000529713.5:n.340T>C
ENST00000531913.1:n.605T>C
NM_000733.3:c.234T>C , LRG_38t1:c.234T>C NP_000724.1:p.Asp78=
NM_000733.4:c.234T>C MANE Select NP_000724.1:p.Asp78=
Search 100 bp 5'
Search 100 bp 3'