Canonical Allele Identifier: CA2616232444

Gene: CD3D

Linked Data

• dbSNP Id: rs2134059256
• gnomAD v4: 11-118339762-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118339762C>T , CM000673.2:g.118339762C>T	GRCh38
NC_000011.9:g.118210477C>T , CM000673.1:g.118210477C>T	GRCh37
NC_000011.8:g.117715687C>T	NCBI36
NG_007566.1:g.419C>T , LRG_39:g.419C>T
NG_009891.1:g.7983G>A , LRG_37:g.7983G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695666.1:n.906G>A
ENST00000695667.1:n.424G>A
ENST00000695668.1:n.2404G>A
ENST00000300692.9:c.406+13G>A MANE Select	ENSP00000300692.4:n.406+13G>A
ENST00000300692.8:c.406+13G>A	ENSP00000300692.4:n.406+13G>A
ENST00000392884.2:c.275-268G>A	ENSP00000376622.2:n.275-268G>A
ENST00000526561.1:n.80-268G>A
ENST00000529594.5:c.187+13G>A	ENSP00000437335.1:n.187+13G>A
ENST00000534687.5:c.288-268G>A
NM_000732.4:c.406+13G>A , LRG_37t1:c.406+13G>A	NP_000723.1:n.406+13G>A
NM_001040651.1:c.275-268G>A	NP_001035741.1:n.275-268G>A
NM_001040651.2:c.275-268G>A	NP_001035741.1:n.275-268G>A
NM_000732.6:c.406+13G>A MANE Select	NP_000723.1:n.406+13G>A