Canonical Allele Identifier: CA2017417784

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13564142G= , CM000674.2:g.13564142G=	GRCh38
NC_000012.11:g.13717076G= , CM000674.1:g.13717076G=	GRCh37
NC_000012.10:g.13608343G=	NCBI36
NG_031854.1:g.420947C=
NG_031854.2:g.422871C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.3096C= MANE Select	ENSP00000477455.1:p.His1032=
ENST00000637214.1:c.69+44461C=	ENSP00000489997.1:n.69+44461C=
ENST00000609686.3:c.3096C=	ENSP00000477455.1:p.His1032=
ENST00000628166.1:n.1356C=
NM_000834.3:c.3096C=	NP_000825.2:p.His1032=
XM_005253351.2:c.882C=	XP_005253408.1:p.His294=
XM_011520628.1:c.3096C=	XP_011518930.1:p.His1032=
XM_011520629.1:c.3096C=	XP_011518931.1:p.His1032=
XM_011520630.1:c.3096C=	XP_011518932.1:p.His1032=
NM_000834.4:c.3096C=	NP_000825.2:p.His1032=
XM_005253351.3:c.882C=	XP_005253408.1:p.His294=
XM_011520628.2:c.3096C=	XP_011518930.1:p.His1032=
XM_011520629.2:c.3096C=	XP_011518931.1:p.His1032=
XM_017019219.2:c.3096C=	XP_016874708.1:p.His1032=
NM_000834.5:c.3096C= MANE Select	NP_000825.2:p.His1032=