Canonical Allele Identifier: CA2017438020

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13563025A= , CM000674.2:g.13563025A=	GRCh38
NC_000012.11:g.13715959A= , CM000674.1:g.13715959A=	GRCh37
NC_000012.10:g.13607226A=	NCBI36
NG_031854.1:g.422064T=
NG_031854.2:g.423988T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.4213T= MANE Select	ENSP00000477455.1:p.Phe1405=
ENST00000637214.1:c.69+45578T=	ENSP00000489997.1:n.69+45578T=
ENST00000609686.3:c.4213T=	ENSP00000477455.1:p.Phe1405=
ENST00000628166.1:n.2473T=
NM_000834.3:c.4213T=	NP_000825.2:p.Phe1405=
XM_005253351.2:c.1999T=	XP_005253408.1:p.Phe667=
XM_011520628.1:c.4213T=	XP_011518930.1:p.Phe1405=
XM_011520629.1:c.4213T=	XP_011518931.1:p.Phe1405=
XM_011520630.1:c.4213T=	XP_011518932.1:p.Phe1405=
NM_000834.4:c.4213T=	NP_000825.2:p.Phe1405=
XM_005253351.3:c.1999T=	XP_005253408.1:p.Phe667=
XM_011520628.2:c.4213T=	XP_011518930.1:p.Phe1405=
XM_011520629.2:c.4213T=	XP_011518931.1:p.Phe1405=
XM_017019219.2:c.4213T=	XP_016874708.1:p.Phe1405=
NM_000834.5:c.4213T= MANE Select	NP_000825.2:p.Phe1405=