Canonical Allele Identifier: CA477081971
Gene: CD3E HGNC NCBI

Linked Data

ClinVar Variation Id: 2761719
ClinVar RCV Id: RCV003583915
dbSNP Id: rs1373408962
MyVariant Identifiers: chr11:g.118183376C>T (hg19) chr11:g.118312661C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312661C>T , CM000673.2:g.118312661C>T GRCh38
NC_000011.9:g.118183376C>T , CM000673.1:g.118183376C>T GRCh37
NC_000011.8:g.117688586C>T NCBI36
NG_007383.1:g.13082C>T , LRG_38:g.13082C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.147C>T MANE Select ENSP00000354566.4:p.Cys49=
ENST00000361763.8:c.147C>T ENSP00000354566.4:p.Cys49=
ENST00000526146.5:n.693C>T
ENST00000528435.5:n.700C>T
ENST00000528600.1:c.129C>T ENSP00000433975.1:p.Cys43=
ENST00000529713.5:n.253C>T
ENST00000531913.1:n.518C>T
NM_000733.3:c.147C>T , LRG_38t1:c.147C>T NP_000724.1:p.Cys49=
NM_000733.4:c.147C>T MANE Select NP_000724.1:p.Cys49=
Search 100 bp 5'
Search 100 bp 3'