Canonical Allele Identifier: CA2017465340

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13617333G= , CM000674.2:g.13617333G=	GRCh38
NC_000012.11:g.13770267G= , CM000674.1:g.13770267G=	GRCh37
NC_000012.10:g.13661534G=	NCBI36
NG_031854.1:g.367756C=
NG_031854.2:g.369680C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1126-676C= MANE Select	ENSP00000477455.1:n.1126-676C=
ENST00000630791.2:c.1126-676C=	ENSP00000486677.2:n.1126-676C=
ENST00000609686.3:c.1126-676C=	ENSP00000477455.1:n.1126-676C=
NM_000834.3:c.1126-676C=	NP_000825.2:n.1126-676C=
XM_011520628.1:c.1126-676C=	XP_011518930.1:n.1126-676C=
XM_011520629.1:c.1126-676C=	XP_011518931.1:n.1126-676C=
XM_011520630.1:c.1126-676C=	XP_011518932.1:n.1126-676C=
XR_931372.1:n.307+2107G=
XR_931373.1:n.447+2107G=
XR_931374.1:n.246+2107G=
NM_000834.4:c.1126-676C=	NP_000825.2:n.1126-676C=
XM_011520628.2:c.1126-676C=	XP_011518930.1:n.1126-676C=
XM_011520629.2:c.1126-676C=	XP_011518931.1:n.1126-676C=
XM_017019219.2:c.1126-676C=	XP_016874708.1:n.1126-676C=
XR_001749013.1:n.728+2107G=
XR_931372.2:n.444+2107G=
XR_931373.2:n.586+2107G=
NM_000834.5:c.1126-676C= MANE Select	NP_000825.2:n.1126-676C=