Canonical Allele Identifier: CA382782687
Gene: CD3E HGNC NCBI

Linked Data

ClinVar Variation Id: 632739
ClinVar RCV Id: RCV000780085
dbSNP Id: rs1565511330
gnomAD v3: 11-118312795-G-C
gnomAD v4: 11-118312795-G-C
MyVariant Identifiers: chr11:g.118183510G>C (hg19) chr11:g.118312795G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312795G>C , CM000673.2:g.118312795G>C GRCh38
NC_000011.9:g.118183510G>C , CM000673.1:g.118183510G>C GRCh37
NC_000011.8:g.117688720G>C NCBI36
NG_007383.1:g.13216G>C , LRG_38:g.13216G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.281G>C MANE Select ENSP00000354566.4:p.Gly94Ala
ENST00000361763.8:c.281G>C ENSP00000354566.4:p.Gly94Ala
ENST00000526146.5:n.827G>C
ENST00000528435.5:n.834G>C
ENST00000528600.1:c.263G>C ENSP00000433975.1:p.Gly88Ala
ENST00000529713.5:n.387G>C
ENST00000531913.1:n.652G>C
NM_000733.3:c.281G>C , LRG_38t1:c.281G>C NP_000724.1:p.Gly94Ala
NM_000733.4:c.281G>C MANE Select NP_000724.1:p.Gly94Ala
Search 100 bp 5'
Search 100 bp 3'