Canonical Allele Identifier: CA2617718349
Gene: GRIN2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13562436_13562437insCTACCTTTGTGCTCACATAGCCTCTTTTTGGTTCTCCC , CM000674.2:g.13562436_13562437insCTACCTTTGTGCTCACATAGCCTCTTTTTGGTTCTCCC GRCh38
NC_000012.11:g.13715370_13715371insCTACCTTTGTGCTCACATAGCCTCTTTTTGGTTCTCCC , CM000674.1:g.13715370_13715371insCTACCTTTGTGCTCACATAGCCTCTTTTTGGTTCTCCC GRCh37
NC_000012.10:g.13606637_13606638insCTACCTTTGTGCTCACATAGCCTCTTTTTGGTTCTCCC NCBI36
NG_031854.1:g.422652_422653insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG
NG_031854.2:g.424576_424577insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG MANE Select ENSP00000477455.1:n.*346_*347insGGGAGAACC...
ENST00000637214.1:c.69+46166_69+46167insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG ENSP00000489997.1:n.69+46166_69+46167insG...
ENST00000609686.3:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG ENSP00000477455.1:n.*346_*347insGGGAGAACC...
NM_000834.3:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG NP_000825.2:n.*346_*347insGGGAGAACCAAAAAG...
XM_005253351.2:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG XP_005253408.1:n.*346_*347insGGGAGAACCAAA...
XM_011520628.1:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG XP_011518930.1:n.*346_*347insGGGAGAACCAAA...
XM_011520629.1:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG XP_011518931.1:n.*346_*347insGGGAGAACCAAA...
XM_011520630.1:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG XP_011518932.1:n.*346_*347insGGGAGAACCAAA...
NM_000834.4:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG NP_000825.2:n.*346_*347insGGGAGAACCAAAAAG...
XM_005253351.3:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG XP_005253408.1:n.*346_*347insGGGAGAACCAAA...
XM_011520628.2:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG XP_011518930.1:n.*346_*347insGGGAGAACCAAA...
XM_011520629.2:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG XP_011518931.1:n.*346_*347insGGGAGAACCAAA...
XM_017019219.2:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG XP_016874708.1:n.*346_*347insGGGAGAACCAAA...
NM_000834.5:c.*346_*347insGGGAGAACCAAAAAGAGGCTATGTGAGCACAAAGGTAG MANE Select NP_000825.2:n.*346_*347insGGGAGAACCAAAAAG...