Canonical Allele Identifier: CA2017464403

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13616545T= , CM000674.2:g.13616545T=	GRCh38
NC_000012.11:g.13769479T= , CM000674.1:g.13769479T=	GRCh37
NC_000012.10:g.13660746T=	NCBI36
NG_031854.1:g.368544A=
NG_031854.2:g.370468A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1238A= MANE Select	ENSP00000477455.1:p.Glu413=
ENST00000630791.2:c.1238A=	ENSP00000486677.2:p.Glu413=
ENST00000609686.3:c.1238A=	ENSP00000477455.1:p.Glu413=
NM_000834.3:c.1238A=	NP_000825.2:p.Glu413=
XM_011520628.1:c.1238A=	XP_011518930.1:p.Glu413=
XM_011520629.1:c.1238A=	XP_011518931.1:p.Glu413=
XM_011520630.1:c.1238A=	XP_011518932.1:p.Glu413=
XR_931372.1:n.307+1319T=
XR_931373.1:n.447+1319T=
XR_931374.1:n.246+1319T=
NM_000834.4:c.1238A=	NP_000825.2:p.Glu413=
XM_011520628.2:c.1238A=	XP_011518930.1:p.Glu413=
XM_011520629.2:c.1238A=	XP_011518931.1:p.Glu413=
XM_017019219.2:c.1238A=	XP_016874708.1:p.Glu413=
XR_001749013.1:n.728+1319T=
XR_931372.2:n.444+1319T=
XR_931373.2:n.586+1319T=
NM_000834.5:c.1238A= MANE Select	NP_000825.2:p.Glu413=