Canonical Allele Identifier: CA382781850
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183372C>G (hg19) chr11:g.118312657C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312657C>G , CM000673.2:g.118312657C>G GRCh38
NC_000011.9:g.118183372C>G , CM000673.1:g.118183372C>G GRCh37
NC_000011.8:g.117688582C>G NCBI36
NG_007383.1:g.13078C>G , LRG_38:g.13078C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.143C>G MANE Select ENSP00000354566.4:p.Thr48Arg
ENST00000361763.8:c.143C>G ENSP00000354566.4:p.Thr48Arg
ENST00000526146.5:n.689C>G
ENST00000528435.5:n.696C>G
ENST00000528600.1:c.125C>G ENSP00000433975.1:p.Thr42Arg
ENST00000529713.5:n.249C>G
ENST00000531913.1:n.514C>G
NM_000733.3:c.143C>G , LRG_38t1:c.143C>G NP_000724.1:p.Thr48Arg
NM_000733.4:c.143C>G MANE Select NP_000724.1:p.Thr48Arg
Search 100 bp 5'
Search 100 bp 3'