Canonical Allele Identifier: CA2017465186

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13617198G= , CM000674.2:g.13617198G=	GRCh38
NC_000012.11:g.13770132G= , CM000674.1:g.13770132G=	GRCh37
NC_000012.10:g.13661399G=	NCBI36
NG_031854.1:g.367891C=
NG_031854.2:g.369815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1126-541C= MANE Select	ENSP00000477455.1:n.1126-541C=
ENST00000630791.2:c.1126-541C=	ENSP00000486677.2:n.1126-541C=
ENST00000609686.3:c.1126-541C=	ENSP00000477455.1:n.1126-541C=
NM_000834.3:c.1126-541C=	NP_000825.2:n.1126-541C=
XM_011520628.1:c.1126-541C=	XP_011518930.1:n.1126-541C=
XM_011520629.1:c.1126-541C=	XP_011518931.1:n.1126-541C=
XM_011520630.1:c.1126-541C=	XP_011518932.1:n.1126-541C=
XR_931372.1:n.307+1972G=
XR_931373.1:n.447+1972G=
XR_931374.1:n.246+1972G=
NM_000834.4:c.1126-541C=	NP_000825.2:n.1126-541C=
XM_011520628.2:c.1126-541C=	XP_011518930.1:n.1126-541C=
XM_011520629.2:c.1126-541C=	XP_011518931.1:n.1126-541C=
XM_017019219.2:c.1126-541C=	XP_016874708.1:n.1126-541C=
XR_001749013.1:n.728+1972G=
XR_931372.2:n.444+1972G=
XR_931373.2:n.586+1972G=
NM_000834.5:c.1126-541C= MANE Select	NP_000825.2:n.1126-541C=