Product Details

SNP ID
rs4764006
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:13537468 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CGAGGCTGTAATCATAAAATGGTGC[C/T]TCCGTTATGTCCATTCTTCAGCTCC
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 30742 Intron NP_000825.2
XM_005253351.3 30742 UTR 3 XP_005253408.1
XM_011520628.2 30742 UTR 3 XP_011518930.1
XM_011520629.2 30742 UTR 3 XP_011518931.1
XM_017019219.1 30742 UTR 3 XP_016874708.1

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