Canonical Allele Identifier: CA6301666
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs748420647
ExAC: 11:118183627 A / G
gnomAD v2: 11-118183627-A-G
gnomAD v4: 11-118312912-A-G
MyVariant Identifiers: chr11:g.118183627A>G (hg19) chr11:g.118312912A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312912A>G , CM000673.2:g.118312912A>G GRCh38
NC_000011.9:g.118183627A>G , CM000673.1:g.118183627A>G GRCh37
NC_000011.8:g.117688837A>G NCBI36
NG_007383.1:g.13333A>G , LRG_38:g.13333A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.352+46A>G MANE Select ENSP00000354566.4:n.352+46A>G
ENST00000361763.8:c.352+46A>G ENSP00000354566.4:n.352+46A>G
ENST00000526146.5:n.944A>G
ENST00000528435.5:n.905+46A>G
ENST00000528600.1:c.334+46A>G ENSP00000433975.1:n.334+46A>G
ENST00000529713.5:n.504A>G
ENST00000531913.1:n.723+46A>G
NM_000733.3:c.352+46A>G , LRG_38t1:c.352+46A>G NP_000724.1:n.352+46A>G
NM_000733.4:c.352+46A>G MANE Select NP_000724.1:n.352+46A>G
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