Product Details

SNP ID
rs4764005
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:13537343 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGAATAGTCACATTTAAGGTCGATT[C/T]CAAGTTTAAATTTTATGTGTAGAAT
Phenotype
MIM: 138252
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
GRIN2B PubMed Links

Gene Details

Gene
GRIN2B
Gene Name
glutamate ionotropic receptor NMDA type subunit 2B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000834.3 30867 Intron NP_000825.2
XM_005253351.3 30867 UTR 3 XP_005253408.1
XM_011520628.2 30867 UTR 3 XP_011518930.1
XM_011520629.2 30867 UTR 3 XP_011518931.1
XM_017019219.1 30867 UTR 3 XP_016874708.1

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