Canonical Allele Identifier: CA2003456997

Gene: CD3D

Linked Data

• dbSNP Id: rs1181662679

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339745C>A , CM000673.2:g.118339745C>A	GRCh38
NC_000011.9:g.118210460C>A , CM000673.1:g.118210460C>A	GRCh37
NC_000011.8:g.117715670C>A	NCBI36
NG_007566.1:g.402C>A , LRG_39:g.402C>A
NG_009891.1:g.8000G>T , LRG_37:g.8000G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.923G>T
ENST00000695667.1:n.441G>T
ENST00000695668.1:n.2421G>T
ENST00000300692.9:c.406+30G>T MANE Select	ENSP00000300692.4:n.406+30G>T
ENST00000300692.8:c.406+30G>T	ENSP00000300692.4:n.406+30G>T
ENST00000392884.2:c.275-251G>T	ENSP00000376622.2:n.275-251G>T
ENST00000526561.1:n.80-251G>T
ENST00000529594.5:c.187+30G>T	ENSP00000437335.1:n.187+30G>T
ENST00000534687.5:c.288-251G>T
NM_000732.4:c.406+30G>T , LRG_37t1:c.406+30G>T	NP_000723.1:n.406+30G>T
NM_001040651.1:c.275-251G>T	NP_001035741.1:n.275-251G>T
NM_001040651.2:c.275-251G>T	NP_001035741.1:n.275-251G>T
NM_000732.6:c.406+30G>T MANE Select	NP_000723.1:n.406+30G>T