Canonical Allele Identifier: CA2017414573

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13563033T= , CM000674.2:g.13563033T=	GRCh38
NC_000012.11:g.13715967T= , CM000674.1:g.13715967T=	GRCh37
NC_000012.10:g.13607234T=	NCBI36
NG_031854.1:g.422056A=
NG_031854.2:g.423980A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.4205A= MANE Select	ENSP00000477455.1:p.Lys1402=
ENST00000637214.1:c.69+45570A=	ENSP00000489997.1:n.69+45570A=
ENST00000609686.3:c.4205A=	ENSP00000477455.1:p.Lys1402=
ENST00000628166.1:n.2465A=
NM_000834.3:c.4205A=	NP_000825.2:p.Lys1402=
XM_005253351.2:c.1991A=	XP_005253408.1:p.Lys664=
XM_011520628.1:c.4205A=	XP_011518930.1:p.Lys1402=
XM_011520629.1:c.4205A=	XP_011518931.1:p.Lys1402=
XM_011520630.1:c.4205A=	XP_011518932.1:p.Lys1402=
NM_000834.4:c.4205A=	NP_000825.2:p.Lys1402=
XM_005253351.3:c.1991A=	XP_005253408.1:p.Lys664=
XM_011520628.2:c.4205A=	XP_011518930.1:p.Lys1402=
XM_011520629.2:c.4205A=	XP_011518931.1:p.Lys1402=
XM_017019219.2:c.4205A=	XP_016874708.1:p.Lys1402=
NM_000834.5:c.4205A= MANE Select	NP_000825.2:p.Lys1402=