Canonical Allele Identifier: CA2017437621

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1948555541

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562306_13562327dup , CM000674.2:g.13562306_13562327dup	GRCh38
NC_000012.11:g.13715240_13715261dup , CM000674.1:g.13715240_13715261dup	GRCh37
NC_000012.10:g.13606507_13606528dup	NCBI36
NG_031854.1:g.422762_422783dup
NG_031854.2:g.424686_424707dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*456_*477dup MANE Select	ENSP00000477455.1:n.*456_*477dup
ENST00000637214.1:c.69+46276_69+46297dup	ENSP00000489997.1:n.69+46276_69+46297dup
ENST00000609686.3:c.*456_*477dup	ENSP00000477455.1:n.*456_*477dup
NM_000834.3:c.*456_*477dup	NP_000825.2:n.*456_*477dup
XM_005253351.2:c.*456_*477dup	XP_005253408.1:n.*456_*477dup
XM_011520628.1:c.*456_*477dup	XP_011518930.1:n.*456_*477dup
XM_011520629.1:c.*456_*477dup	XP_011518931.1:n.*456_*477dup
XM_011520630.1:c.*456_*477dup	XP_011518932.1:n.*456_*477dup
NM_000834.4:c.*456_*477dup	NP_000825.2:n.*456_*477dup
XM_005253351.3:c.*456_*477dup	XP_005253408.1:n.*456_*477dup
XM_011520628.2:c.*456_*477dup	XP_011518930.1:n.*456_*477dup
XM_011520629.2:c.*456_*477dup	XP_011518931.1:n.*456_*477dup
XM_017019219.2:c.*456_*477dup	XP_016874708.1:n.*456_*477dup
NM_000834.5:c.*456_*477dup MANE Select	NP_000825.2:n.*456_*477dup