Canonical Allele Identifier: CA601878014

Gene: CD3D

Linked Data

• dbSNP Id: rs369069455
• gnomAD v2: 11-118210466-C-A
• gnomAD v4: 11-118339751-C-A
• MyVariant Identifiers: chr11:g.118210466C>A (hg19) ; chr11:g.118339751C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339751C>A , CM000673.2:g.118339751C>A	GRCh38
NC_000011.9:g.118210466C>A , CM000673.1:g.118210466C>A	GRCh37
NC_000011.8:g.117715676C>A	NCBI36
NG_007566.1:g.408C>A , LRG_39:g.408C>A
NG_009891.1:g.7994G>T , LRG_37:g.7994G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.917G>T
ENST00000695667.1:n.435G>T
ENST00000695668.1:n.2415G>T
ENST00000300692.9:c.406+24G>T MANE Select	ENSP00000300692.4:n.406+24G>T
ENST00000300692.8:c.406+24G>T	ENSP00000300692.4:n.406+24G>T
ENST00000392884.2:c.275-257G>T	ENSP00000376622.2:n.275-257G>T
ENST00000526561.1:n.80-257G>T
ENST00000529594.5:c.187+24G>T	ENSP00000437335.1:n.187+24G>T
ENST00000534687.5:c.288-257G>T
NM_000732.4:c.406+24G>T , LRG_37t1:c.406+24G>T	NP_000723.1:n.406+24G>T
NM_001040651.1:c.275-257G>T	NP_001035741.1:n.275-257G>T
NM_001040651.2:c.275-257G>T	NP_001035741.1:n.275-257G>T
NM_000732.6:c.406+24G>T MANE Select	NP_000723.1:n.406+24G>T