Canonical Allele Identifier: CA6301642
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs148647954
ExAC: 11:118183440 G / T
gnomAD v2: 11-118183440-G-T
gnomAD v3: 11-118312725-G-T
gnomAD v4: 11-118312725-G-T
MyVariant Identifiers: chr11:g.118183440G>T (hg19) chr11:g.118312725G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312725G>T , CM000673.2:g.118312725G>T GRCh38
NC_000011.9:g.118183440G>T , CM000673.1:g.118183440G>T GRCh37
NC_000011.8:g.117688650G>T NCBI36
NG_007383.1:g.13146G>T , LRG_38:g.13146G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.211G>T MANE Select ENSP00000354566.4:p.Asp71Tyr
ENST00000361763.8:c.211G>T ENSP00000354566.4:p.Asp71Tyr
ENST00000526146.5:n.757G>T
ENST00000528435.5:n.764G>T
ENST00000528600.1:c.193G>T ENSP00000433975.1:p.Asp65Tyr
ENST00000529713.5:n.317G>T
ENST00000531913.1:n.582G>T
NM_000733.3:c.211G>T , LRG_38t1:c.211G>T NP_000724.1:p.Asp71Tyr
NM_000733.4:c.211G>T MANE Select NP_000724.1:p.Asp71Tyr
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