Product Details

SNP ID
rs4764008
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:13543308 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCTCCAACCCACCTCCTAATTTCTA[C/G]GTTATTGCTTCTGACTCACTAACTG
Phenotype
MIM: 138252
Polymorphism
C/G, Transversion 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 24902 Intron NP_000825.2
XM_005253351.3 24902 UTR 3 XP_005253408.1
XM_011520628.2 24902 UTR 3 XP_011518930.1
XM_011520629.2 24902 UTR 3 XP_011518931.1
XM_017019219.1 24902 UTR 3 XP_016874708.1

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