Canonical Allele Identifier: CA382782732
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183515T>C (hg19) chr11:g.118312800T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312800T>C , CM000673.2:g.118312800T>C GRCh38
NC_000011.9:g.118183515T>C , CM000673.1:g.118183515T>C GRCh37
NC_000011.8:g.117688725T>C NCBI36
NG_007383.1:g.13221T>C , LRG_38:g.13221T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.286T>C MANE Select ENSP00000354566.4:p.Tyr96His
ENST00000361763.8:c.286T>C ENSP00000354566.4:p.Tyr96His
ENST00000526146.5:n.832T>C
ENST00000528435.5:n.839T>C
ENST00000528600.1:c.268T>C ENSP00000433975.1:p.Tyr90His
ENST00000529713.5:n.392T>C
ENST00000531913.1:n.657T>C
NM_000733.3:c.286T>C , LRG_38t1:c.286T>C NP_000724.1:p.Tyr96His
NM_000733.4:c.286T>C MANE Select NP_000724.1:p.Tyr96His
Search 100 bp 5'
Search 100 bp 3'