Canonical Allele Identifier: CA477082505
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs939153709
MyVariant Identifiers: chr11:g.118183433T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312718T>G , CM000673.2:g.118312718T>G GRCh38
NC_000011.9:g.118183433T>G , CM000673.1:g.118183433T>G GRCh37
NC_000011.8:g.117688643T>G NCBI36
NG_007383.1:g.13139T>G , LRG_38:g.13139T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.204T>G MANE Select ENSP00000354566.4:p.Gly68=
ENST00000361763.8:c.204T>G ENSP00000354566.4:p.Gly68=
ENST00000526146.5:n.750T>G
ENST00000528435.5:n.757T>G
ENST00000528600.1:c.186T>G ENSP00000433975.1:p.Gly62=
ENST00000529713.5:n.310T>G
ENST00000531913.1:n.575T>G
NM_000733.3:c.204T>G , LRG_38t1:c.204T>G NP_000724.1:p.Gly68=
NM_000733.4:c.204T>G MANE Select NP_000724.1:p.Gly68=