Canonical Allele Identifier: CA2017437051

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561261G= , CM000674.2:g.13561261G=	GRCh38
NC_000012.11:g.13714195G= , CM000674.1:g.13714195G=	GRCh37
NC_000012.10:g.13605462G=	NCBI36
NG_031854.1:g.423828C=
NG_031854.2:g.425752C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1522C= MANE Select	ENSP00000477455.1:n.*1522C=
ENST00000637214.1:c.69+47342C=	ENSP00000489997.1:n.69+47342C=
ENST00000609686.3:c.*1522C=	ENSP00000477455.1:n.*1522C=
XM_005253351.2:c.*1522C=	XP_005253408.1:n.*1522C=
XM_011520628.1:c.*1522C=	XP_011518930.1:n.*1522C=
XM_011520629.1:c.*1522C=	XP_011518931.1:n.*1522C=
XM_011520630.1:c.*1522C=	XP_011518932.1:n.*1522C=
NM_000834.4:c.*1522C=	NP_000825.2:n.*1522C=
XM_005253351.3:c.*1522C=	XP_005253408.1:n.*1522C=
XM_011520628.2:c.*1522C=	XP_011518930.1:n.*1522C=
XM_011520629.2:c.*1522C=	XP_011518931.1:n.*1522C=
XM_017019219.2:c.*1522C=	XP_016874708.1:n.*1522C=
NM_000834.5:c.*1522C= MANE Select	NP_000825.2:n.*1522C=