Canonical Allele Identifier: CA2017441428

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13571945A= , CM000674.2:g.13571945A=	GRCh38
NC_000012.11:g.13724879A= , CM000674.1:g.13724879A=	GRCh37
NC_000012.10:g.13616146A=	NCBI36
NG_031854.1:g.413144T=
NG_031854.2:g.415068T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.2030T= MANE Select	ENSP00000477455.1:p.Phe677=
ENST00000628166.2:n.290T=
ENST00000637214.1:c.69+36658T=	ENSP00000489997.1:n.69+36658T=
ENST00000609686.3:c.2030T=	ENSP00000477455.1:p.Phe677=
ENST00000628166.1:n.290T=
NM_000834.3:c.2030T=	NP_000825.2:p.Phe677=
XM_005253351.2:c.-43-1928T=	XP_005253408.1:n.-43-1928T=
XM_011520628.1:c.2030T=	XP_011518930.1:p.Phe677=
XM_011520629.1:c.2030T=	XP_011518931.1:p.Phe677=
XM_011520630.1:c.2030T=	XP_011518932.1:p.Phe677=
NM_000834.4:c.2030T=	NP_000825.2:p.Phe677=
XM_005253351.3:c.-43-1928T=	XP_005253408.1:n.-43-1928T=
XM_011520628.2:c.2030T=	XP_011518930.1:p.Phe677=
XM_011520629.2:c.2030T=	XP_011518931.1:p.Phe677=
XM_017019219.2:c.2030T=	XP_016874708.1:p.Phe677=
NM_000834.5:c.2030T= MANE Select	NP_000825.2:p.Phe677=