Canonical Allele Identifier: CA2017489189

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13675353T= , CM000674.2:g.13675353T=	GRCh38
NC_000012.11:g.13828287T= , CM000674.1:g.13828287T=	GRCh37
NC_000012.10:g.13719554T=	NCBI36
NG_031854.1:g.309736A=
NG_031854.2:g.311660A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000834.5:c.1125+392A= MANE Select	NP_000825.2:n.1125+392A=
ENST00000609686.4:c.1125+392A= MANE Select	ENSP00000477455.1:n.1125+392A=
NM_000834.3:c.1125+392A=	NP_000825.2:n.1125+392A=
NM_000834.4:c.1125+392A=	NP_000825.2:n.1125+392A=
ENST00000609686.3:c.1125+392A=	ENSP00000477455.1:n.1125+392A=
ENST00000630791.2:c.1125+392A=	ENSP00000486677.2:n.1125+392A=
ENST00000636855.1:n.23+392A=
ENST00000636856.1:n.76+392A=
XM_011520628.1:c.1125+392A=	XP_011518930.1:n.1125+392A=
XM_011520628.2:c.1125+392A=	XP_011518930.1:n.1125+392A=
XM_011520629.1:c.1125+392A=	XP_011518931.1:n.1125+392A=
XM_011520629.2:c.1125+392A=	XP_011518931.1:n.1125+392A=
XM_011520630.1:c.1125+392A=	XP_011518932.1:n.1125+392A=
XM_017019219.2:c.1125+392A=	XP_016874708.1:n.1125+392A=