Canonical Allele Identifier: CA382782766
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183522G>C (hg19) chr11:g.118312807G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312807G>C , CM000673.2:g.118312807G>C GRCh38
NC_000011.9:g.118183522G>C , CM000673.1:g.118183522G>C GRCh37
NC_000011.8:g.117688732G>C NCBI36
NG_007383.1:g.13228G>C , LRG_38:g.13228G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.293G>C MANE Select ENSP00000354566.4:p.Cys98Ser
ENST00000361763.8:c.293G>C ENSP00000354566.4:p.Cys98Ser
ENST00000526146.5:n.839G>C
ENST00000528435.5:n.846G>C
ENST00000528600.1:c.275G>C ENSP00000433975.1:p.Cys92Ser
ENST00000529713.5:n.399G>C
ENST00000531913.1:n.664G>C
NM_000733.3:c.293G>C , LRG_38t1:c.293G>C NP_000724.1:p.Cys98Ser
NM_000733.4:c.293G>C MANE Select NP_000724.1:p.Cys98Ser
Search 100 bp 5'
Search 100 bp 3'