Canonical Allele Identifier: CA2017437060

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561284T= , CM000674.2:g.13561284T=	GRCh38
NC_000012.11:g.13714218T= , CM000674.1:g.13714218T=	GRCh37
NC_000012.10:g.13605485T=	NCBI36
NG_031854.1:g.423805A=
NG_031854.2:g.425729A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*1499A= MANE Select	ENSP00000477455.1:n.*1499A=
ENST00000637214.1:c.69+47319A=	ENSP00000489997.1:n.69+47319A=
ENST00000609686.3:c.*1499A=	ENSP00000477455.1:n.*1499A=
XM_005253351.2:c.*1499A=	XP_005253408.1:n.*1499A=
XM_011520628.1:c.*1499A=	XP_011518930.1:n.*1499A=
XM_011520629.1:c.*1499A=	XP_011518931.1:n.*1499A=
XM_011520630.1:c.*1499A=	XP_011518932.1:n.*1499A=
NM_000834.4:c.*1499A=	NP_000825.2:n.*1499A=
XM_005253351.3:c.*1499A=	XP_005253408.1:n.*1499A=
XM_011520628.2:c.*1499A=	XP_011518930.1:n.*1499A=
XM_011520629.2:c.*1499A=	XP_011518931.1:n.*1499A=
XM_017019219.2:c.*1499A=	XP_016874708.1:n.*1499A=
NM_000834.5:c.*1499A= MANE Select	NP_000825.2:n.*1499A=