Canonical Allele Identifier: CA477081979
Gene: CD3E HGNC NCBI

Linked Data

dbSNP Id: rs1948142165
MyVariant Identifiers: chr11:g.118183391A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312676A>T , CM000673.2:g.118312676A>T GRCh38
NC_000011.9:g.118183391A>T , CM000673.1:g.118183391A>T GRCh37
NC_000011.8:g.117688601A>T NCBI36
NG_007383.1:g.13097A>T , LRG_38:g.13097A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.162A>T MANE Select ENSP00000354566.4:p.Gly54=
ENST00000361763.8:c.162A>T ENSP00000354566.4:p.Gly54=
ENST00000526146.5:n.708A>T
ENST00000528435.5:n.715A>T
ENST00000528600.1:c.144A>T ENSP00000433975.1:p.Gly48=
ENST00000529713.5:n.268A>T
ENST00000531913.1:n.533A>T
NM_000733.3:c.162A>T , LRG_38t1:c.162A>T NP_000724.1:p.Gly54=
NM_000733.4:c.162A>T MANE Select NP_000724.1:p.Gly54=