Canonical Allele Identifier: CA2017509997

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13718984T= , CM000674.2:g.13718984T=	GRCh38
NC_000012.11:g.13871918T= , CM000674.1:g.13871918T=	GRCh37
NC_000012.10:g.13763185T=	NCBI36
NG_031854.1:g.266105A=
NG_031854.2:g.268029A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1010+34333A= MANE Select	ENSP00000477455.1:n.1010+34333A=
ENST00000630791.2:c.1010+34333A=	ENSP00000486677.2:n.1010+34333A=
ENST00000609686.3:c.1010+34333A=	ENSP00000477455.1:n.1010+34333A=
NM_000834.3:c.1010+34333A=	NP_000825.2:n.1010+34333A=
XM_011520628.1:c.1010+34333A=	XP_011518930.1:n.1010+34333A=
XM_011520629.1:c.1010+34333A=	XP_011518931.1:n.1010+34333A=
XM_011520630.1:c.1010+34333A=	XP_011518932.1:n.1010+34333A=
NM_000834.4:c.1010+34333A=	NP_000825.2:n.1010+34333A=
XM_011520628.2:c.1010+34333A=	XP_011518930.1:n.1010+34333A=
XM_011520629.2:c.1010+34333A=	XP_011518931.1:n.1010+34333A=
XM_017019219.2:c.1010+34333A=	XP_016874708.1:n.1010+34333A=
NM_000834.5:c.1010+34333A= MANE Select	NP_000825.2:n.1010+34333A=