Canonical Allele Identifier: CA2017463490

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615664C= , CM000674.2:g.13615664C=	GRCh38
NC_000012.11:g.13768598C= , CM000674.1:g.13768598C=	GRCh37
NC_000012.10:g.13659865C=	NCBI36
NG_031854.1:g.369425G=
NG_031854.2:g.371349G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1329G= MANE Select	ENSP00000477455.1:p.Glu443=
ENST00000630791.2:c.1329G=	ENSP00000486677.2:p.Glu443=
ENST00000609686.3:c.1329G=	ENSP00000477455.1:p.Glu443=
NM_000834.3:c.1329G=	NP_000825.2:p.Glu443=
XM_011520628.1:c.1329G=	XP_011518930.1:p.Glu443=
XM_011520629.1:c.1329G=	XP_011518931.1:p.Glu443=
XM_011520630.1:c.1329G=	XP_011518932.1:p.Glu443=
XR_931372.1:n.307+438C=
XR_931373.1:n.447+438C=
XR_931374.1:n.246+438C=
NM_000834.4:c.1329G=	NP_000825.2:p.Glu443=
XM_011520628.2:c.1329G=	XP_011518930.1:p.Glu443=
XM_011520629.2:c.1329G=	XP_011518931.1:p.Glu443=
XM_017019219.2:c.1329G=	XP_016874708.1:p.Glu443=
XR_001749013.1:n.728+438C=
XR_931372.2:n.444+438C=
XR_931373.2:n.586+438C=
NM_000834.5:c.1329G= MANE Select	NP_000825.2:p.Glu443=