Canonical Allele Identifier: CA2017436943

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1948536399

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561054_13561057dup , CM000674.2:g.13561054_13561057dup	GRCh38
NC_000012.11:g.13713988_13713991dup , CM000674.1:g.13713988_13713991dup	GRCh37
NC_000012.10:g.13605255_13605258dup	NCBI36
NG_031854.1:g.424034_424037dup
NG_031854.2:g.425958_425961dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1728_*1731dup MANE Select	ENSP00000477455.1:n.*1728_*1731dup
ENST00000637214.1:c.69+47548_69+47551dup	ENSP00000489997.1:n.69+47548_69+47551dup
ENST00000609686.3:c.*1728_*1731dup	ENSP00000477455.1:n.*1728_*1731dup
XM_005253351.2:c.*1728_*1731dup	XP_005253408.1:n.*1728_*1731dup
XM_011520628.1:c.*1728_*1731dup	XP_011518930.1:n.*1728_*1731dup
XM_011520629.1:c.*1728_*1731dup	XP_011518931.1:n.*1728_*1731dup
XM_011520630.1:c.*1728_*1731dup	XP_011518932.1:n.*1728_*1731dup
NM_000834.4:c.*1728_*1731dup	NP_000825.2:n.*1728_*1731dup
XM_005253351.3:c.*1728_*1731dup	XP_005253408.1:n.*1728_*1731dup
XM_011520628.2:c.*1728_*1731dup	XP_011518930.1:n.*1728_*1731dup
XM_011520629.2:c.*1728_*1731dup	XP_011518931.1:n.*1728_*1731dup
XM_017019219.2:c.*1728_*1731dup	XP_016874708.1:n.*1728_*1731dup
NM_000834.5:c.*1728_*1731dup MANE Select	NP_000825.2:n.*1728_*1731dup