Canonical Allele Identifier: CA2017526038

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753963C= , CM000674.2:g.13753963C=	GRCh38
NC_000012.11:g.13906897C= , CM000674.1:g.13906897C=	GRCh37
NC_000012.10:g.13798164C=	NCBI36
NG_031854.1:g.231126G=
NG_031854.2:g.233050G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.412-48G= MANE Select	ENSP00000477455.1:n.412-48G=
ENST00000630791.2:c.412-48G=	ENSP00000486677.2:n.412-48G=
ENST00000609686.3:c.412-48G=	ENSP00000477455.1:n.412-48G=
NM_000834.3:c.412-48G=	NP_000825.2:n.412-48G=
XM_011520628.1:c.412-48G=	XP_011518930.1:n.412-48G=
XM_011520629.1:c.412-48G=	XP_011518931.1:n.412-48G=
XM_011520630.1:c.412-48G=	XP_011518932.1:n.412-48G=
NM_000834.4:c.412-48G=	NP_000825.2:n.412-48G=
XM_011520628.2:c.412-48G=	XP_011518930.1:n.412-48G=
XM_011520629.2:c.412-48G=	XP_011518931.1:n.412-48G=
XM_017019219.2:c.412-48G=	XP_016874708.1:n.412-48G=
NM_000834.5:c.412-48G= MANE Select	NP_000825.2:n.412-48G=