Canonical Allele Identifier: CA2017447580

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608577C= , CM000674.2:g.13608577C=	GRCh38
NC_000012.11:g.13761511C= , CM000674.1:g.13761511C=	GRCh37
NC_000012.10:g.13652778C=	NCBI36
NG_031854.1:g.376512G=
NG_031854.2:g.378436G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.2010+26G= MANE Select	ENSP00000477455.1:n.2010+26G=
ENST00000628166.2:n.270+26G=
ENST00000637214.1:c.69+26G=	ENSP00000489997.1:n.69+26G=
ENST00000609686.3:c.2010+26G=	ENSP00000477455.1:n.2010+26G=
ENST00000628166.1:n.270+26G=
NM_000834.3:c.2010+26G=	NP_000825.2:n.2010+26G=
XM_005253351.2:c.-44+26G=	XP_005253408.1:n.-44+26G=
XM_011520628.1:c.2010+26G=	XP_011518930.1:n.2010+26G=
XM_011520629.1:c.2010+26G=	XP_011518931.1:n.2010+26G=
XM_011520630.1:c.2010+26G=	XP_011518932.1:n.2010+26G=
XR_931372.1:n.179-6521C=
XR_931373.1:n.179-41C=
NM_000834.4:c.2010+26G=	NP_000825.2:n.2010+26G=
XM_005253351.3:c.-44+26G=	XP_005253408.1:n.-44+26G=
XM_011520628.2:c.2010+26G=	XP_011518930.1:n.2010+26G=
XM_011520629.2:c.2010+26G=	XP_011518931.1:n.2010+26G=
XM_017019219.2:c.2010+26G=	XP_016874708.1:n.2010+26G=
XR_001749013.1:n.318-41C=
XR_931372.2:n.316-6521C=
XR_931373.2:n.318-41C=
NM_000834.5:c.2010+26G= MANE Select	NP_000825.2:n.2010+26G=