Canonical Allele Identifier: CA2017437607

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562284G= , CM000674.2:g.13562284G=	GRCh38
NC_000012.11:g.13715218G= , CM000674.1:g.13715218G=	GRCh37
NC_000012.10:g.13606485G=	NCBI36
NG_031854.1:g.422805C=
NG_031854.2:g.424729C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*499C= MANE Select	ENSP00000477455.1:n.*499C=
ENST00000636207.1:n.8C=
ENST00000637214.1:c.69+46319C=	ENSP00000489997.1:n.69+46319C=
ENST00000609686.3:c.*499C=	ENSP00000477455.1:n.*499C=
NM_000834.3:c.*499C=	NP_000825.2:n.*499C=
XM_005253351.2:c.*499C=	XP_005253408.1:n.*499C=
XM_011520628.1:c.*499C=	XP_011518930.1:n.*499C=
XM_011520629.1:c.*499C=	XP_011518931.1:n.*499C=
XM_011520630.1:c.*499C=	XP_011518932.1:n.*499C=
NM_000834.4:c.*499C=	NP_000825.2:n.*499C=
XM_005253351.3:c.*499C=	XP_005253408.1:n.*499C=
XM_011520628.2:c.*499C=	XP_011518930.1:n.*499C=
XM_011520629.2:c.*499C=	XP_011518931.1:n.*499C=
XM_017019219.2:c.*499C=	XP_016874708.1:n.*499C=
NM_000834.5:c.*499C= MANE Select	NP_000825.2:n.*499C=