Canonical Allele Identifier: CA2017614121

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13944910G= , CM000674.2:g.13944910G=	GRCh38
NC_000012.11:g.14097844G= , CM000674.1:g.14097844G=	GRCh37
NC_000012.10:g.13989111G=	NCBI36
NG_031854.1:g.40179C=
NG_031854.2:g.42103C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-19+35018C= MANE Select	ENSP00000477455.1:n.-19+35018C=
ENST00000630791.2:c.-19+35018C=	ENSP00000486677.2:n.-19+35018C=
ENST00000609686.3:c.-19+35018C=	ENSP00000477455.1:n.-19+35018C=
ENST00000627535.2:c.-19+35018C=	ENSP00000486411.1:n.-19+35018C=
ENST00000630791.1:c.-19+35018C=	ENSP00000486677.1:n.-19+35018C=
NM_000834.3:c.-19+35018C=	NP_000825.2:n.-19+35018C=
XM_011520628.1:c.-19+35018C=	XP_011518930.1:n.-19+35018C=
XM_011520629.1:c.-19+35018C=	XP_011518931.1:n.-19+35018C=
XM_011520630.1:c.-19+35018C=	XP_011518932.1:n.-19+35018C=
NM_000834.4:c.-19+35018C=	NP_000825.2:n.-19+35018C=
XM_011520628.2:c.-19+35018C=	XP_011518930.1:n.-19+35018C=
XM_011520629.2:c.-19+35018C=	XP_011518931.1:n.-19+35018C=
XM_017019219.2:c.-19+35018C=	XP_016874708.1:n.-19+35018C=
NM_000834.5:c.-19+35018C= MANE Select	NP_000825.2:n.-19+35018C=