Canonical Allele Identifier: CA6301638

Gene: CD3E

Linked Data

• ClinVar Variation Id: 2901635
• ClinVar RCV Id: RCV003745067
• dbSNP Id: rs188934551
• ExAC: 11:118183430 C / T
• gnomAD v2: 11-118183430-C-T
• gnomAD v3: 11-118312715-C-T
• gnomAD v4: 11-118312715-C-T
• MyVariant Identifiers: chr11:g.118183430C>T (hg19) ; chr11:g.118312715C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118312715C>T , CM000673.2:g.118312715C>T	GRCh38
NC_000011.9:g.118183430C>T , CM000673.1:g.118183430C>T	GRCh37
NC_000011.8:g.117688640C>T	NCBI36
NG_007383.1:g.13136C>T , LRG_38:g.13136C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361763.9:c.201C>T MANE Select	ENSP00000354566.4:p.Gly67=
ENST00000361763.8:c.201C>T	ENSP00000354566.4:p.Gly67=
ENST00000526146.5:n.747C>T
ENST00000528435.5:n.754C>T
ENST00000528600.1:c.183C>T	ENSP00000433975.1:p.Gly61=
ENST00000529713.5:n.307C>T
ENST00000531913.1:n.572C>T
NM_000733.3:c.201C>T , LRG_38t1:c.201C>T	NP_000724.1:p.Gly67=
NM_000733.4:c.201C>T MANE Select	NP_000724.1:p.Gly67=