Canonical Allele Identifier: CA477081982
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs1591269035
MyVariant Identifiers: chr11:g.118183394T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312679T>G , CM000673.2:g.118312679T>G GRCh38
NC_000011.9:g.118183394T>G , CM000673.1:g.118183394T>G GRCh37
NC_000011.8:g.117688604T>G NCBI36
NG_007383.1:g.13100T>G , LRG_38:g.13100T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.165T>G MANE Select ENSP00000354566.4:p.Ser55=
ENST00000361763.8:c.165T>G ENSP00000354566.4:p.Ser55=
ENST00000526146.5:n.711T>G
ENST00000528435.5:n.718T>G
ENST00000528600.1:c.147T>G ENSP00000433975.1:p.Ser49=
ENST00000529713.5:n.271T>G
ENST00000531913.1:n.536T>G
NM_000733.3:c.165T>G , LRG_38t1:c.165T>G NP_000724.1:p.Ser55=
NM_000733.4:c.165T>G MANE Select NP_000724.1:p.Ser55=
Search 100 bp 5'
Search 100 bp 3'