Canonical Allele Identifier: CA2017525832

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753450C= , CM000674.2:g.13753450C=	GRCh38
NC_000012.11:g.13906384C= , CM000674.1:g.13906384C=	GRCh37
NC_000012.10:g.13797651C=	NCBI36
NG_031854.1:g.231639G=
NG_031854.2:g.233563G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.877G= MANE Select	ENSP00000477455.1:p.Val293=
ENST00000630791.2:c.877G=	ENSP00000486677.2:p.Val293=
ENST00000609686.3:c.877G=	ENSP00000477455.1:p.Val293=
NM_000834.3:c.877G=	NP_000825.2:p.Val293=
XM_011520628.1:c.877G=	XP_011518930.1:p.Val293=
XM_011520629.1:c.877G=	XP_011518931.1:p.Val293=
XM_011520630.1:c.877G=	XP_011518932.1:p.Val293=
NM_000834.4:c.877G=	NP_000825.2:p.Val293=
XM_011520628.2:c.877G=	XP_011518930.1:p.Val293=
XM_011520629.2:c.877G=	XP_011518931.1:p.Val293=
XM_017019219.2:c.877G=	XP_016874708.1:p.Val293=
NM_000834.5:c.877G= MANE Select	NP_000825.2:p.Val293=