Canonical Allele Identifier: CA233131013
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1041395268

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13561068_13561071dup , CM000674.2:g.13561068_13561071dup GRCh38
NC_000012.11:g.13714002_13714005dup , CM000674.1:g.13714002_13714005dup GRCh37
NC_000012.10:g.13605269_13605272dup NCBI36
NG_031854.1:g.424022_424025dup
NG_031854.2:g.425946_425949dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.*1716_*1719dup MANE Select ENSP00000477455.1:n.*1716_*1719dup
ENST00000637214.1:c.69+47536_69+47539dup ENSP00000489997.1:n.69+47536_69+47539dup
ENST00000609686.3:c.*1716_*1719dup ENSP00000477455.1:n.*1716_*1719dup
XM_005253351.2:c.*1716_*1719dup XP_005253408.1:n.*1716_*1719dup
XM_011520628.1:c.*1716_*1719dup XP_011518930.1:n.*1716_*1719dup
XM_011520629.1:c.*1716_*1719dup XP_011518931.1:n.*1716_*1719dup
XM_011520630.1:c.*1716_*1719dup XP_011518932.1:n.*1716_*1719dup
NM_000834.4:c.*1716_*1719dup NP_000825.2:n.*1716_*1719dup
XM_005253351.3:c.*1716_*1719dup XP_005253408.1:n.*1716_*1719dup
XM_011520628.2:c.*1716_*1719dup XP_011518930.1:n.*1716_*1719dup
XM_011520629.2:c.*1716_*1719dup XP_011518931.1:n.*1716_*1719dup
XM_017019219.2:c.*1716_*1719dup XP_016874708.1:n.*1716_*1719dup
NM_000834.5:c.*1716_*1719dup MANE Select NP_000825.2:n.*1716_*1719dup