Canonical Allele Identifier: CA2017417153

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13563906C= , CM000674.2:g.13563906C=	GRCh38
NC_000012.11:g.13716840C= , CM000674.1:g.13716840C=	GRCh37
NC_000012.10:g.13608107C=	NCBI36
NG_031854.1:g.421183G=
NG_031854.2:g.423107G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000834.5:c.3332G= MANE Select	NP_000825.2:p.Arg1111=
ENST00000609686.4:c.3332G= MANE Select	ENSP00000477455.1:p.Arg1111=
NM_000834.3:c.3332G=	NP_000825.2:p.Arg1111=
NM_000834.4:c.3332G=	NP_000825.2:p.Arg1111=
ENST00000609686.3:c.3332G=	ENSP00000477455.1:p.Arg1111=
ENST00000628166.1:n.1592G=
ENST00000637214.1:c.69+44697G=	ENSP00000489997.1:n.69+44697G=
XM_005253351.2:c.1118G=	XP_005253408.1:p.Arg373=
XM_005253351.3:c.1118G=	XP_005253408.1:p.Arg373=
XM_011520628.1:c.3332G=	XP_011518930.1:p.Arg1111=
XM_011520628.2:c.3332G=	XP_011518930.1:p.Arg1111=
XM_011520629.1:c.3332G=	XP_011518931.1:p.Arg1111=
XM_011520629.2:c.3332G=	XP_011518931.1:p.Arg1111=
XM_011520630.1:c.3332G=	XP_011518932.1:p.Arg1111=
XM_017019219.2:c.3332G=	XP_016874708.1:p.Arg1111=