Canonical Allele Identifier: CA477082602
Gene: CD3E HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.118183472C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118312757C>T , CM000673.2:g.118312757C>T GRCh38
NC_000011.9:g.118183472C>T , CM000673.1:g.118183472C>T GRCh37
NC_000011.8:g.117688682C>T NCBI36
NG_007383.1:g.13178C>T , LRG_38:g.13178C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361763.9:c.243C>T MANE Select ENSP00000354566.4:p.His81=
ENST00000361763.8:c.243C>T ENSP00000354566.4:p.His81=
ENST00000526146.5:n.789C>T
ENST00000528435.5:n.796C>T
ENST00000528600.1:c.225C>T ENSP00000433975.1:p.His75=
ENST00000529713.5:n.349C>T
ENST00000531913.1:n.614C>T
NM_000733.3:c.243C>T , LRG_38t1:c.243C>T NP_000724.1:p.His81=
NM_000733.4:c.243C>T MANE Select NP_000724.1:p.His81=