Canonical Allele Identifier: CA2017418278

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13564302T= , CM000674.2:g.13564302T=	GRCh38
NC_000012.11:g.13717236T= , CM000674.1:g.13717236T=	GRCh37
NC_000012.10:g.13608503T=	NCBI36
NG_031854.1:g.420787A=
NG_031854.2:g.422711A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.2936A= MANE Select	ENSP00000477455.1:p.Asn979=
ENST00000637214.1:c.69+44301A=	ENSP00000489997.1:n.69+44301A=
ENST00000609686.3:c.2936A=	ENSP00000477455.1:p.Asn979=
ENST00000628166.1:n.1196A=
NM_000834.3:c.2936A=	NP_000825.2:p.Asn979=
XM_005253351.2:c.722A=	XP_005253408.1:p.Asn241=
XM_011520628.1:c.2936A=	XP_011518930.1:p.Asn979=
XM_011520629.1:c.2936A=	XP_011518931.1:p.Asn979=
XM_011520630.1:c.2936A=	XP_011518932.1:p.Asn979=
NM_000834.4:c.2936A=	NP_000825.2:p.Asn979=
XM_005253351.3:c.722A=	XP_005253408.1:p.Asn241=
XM_011520628.2:c.2936A=	XP_011518930.1:p.Asn979=
XM_011520629.2:c.2936A=	XP_011518931.1:p.Asn979=
XM_017019219.2:c.2936A=	XP_016874708.1:p.Asn979=
NM_000834.5:c.2936A= MANE Select	NP_000825.2:p.Asn979=