Canonical Allele Identifier: CA2617717739
Gene: GRIN2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13561300dup , CM000674.2:g.13561300dup GRCh38
NC_000012.11:g.13714234dup , CM000674.1:g.13714234dup GRCh37
NC_000012.10:g.13605501dup NCBI36
NG_031854.1:g.423790dup
NG_031854.2:g.425714dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.*1484dup MANE Select ENSP00000477455.1:n.*1484dup
ENST00000637214.1:c.69+47304dup ENSP00000489997.1:n.69+47304dup
ENST00000609686.3:c.*1484dup ENSP00000477455.1:n.*1484dup
XM_005253351.2:c.*1484dup XP_005253408.1:n.*1484dup
XM_011520628.1:c.*1484dup XP_011518930.1:n.*1484dup
XM_011520629.1:c.*1484dup XP_011518931.1:n.*1484dup
XM_011520630.1:c.*1484dup XP_011518932.1:n.*1484dup
NM_000834.4:c.*1484dup NP_000825.2:n.*1484dup
XM_005253351.3:c.*1484dup XP_005253408.1:n.*1484dup
XM_011520628.2:c.*1484dup XP_011518930.1:n.*1484dup
XM_011520629.2:c.*1484dup XP_011518931.1:n.*1484dup
XM_017019219.2:c.*1484dup XP_016874708.1:n.*1484dup
NM_000834.5:c.*1484dup MANE Select NP_000825.2:n.*1484dup