Canonical Allele Identifier: CA2017437065

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561291A= , CM000674.2:g.13561291A=	GRCh38
NC_000012.11:g.13714225A= , CM000674.1:g.13714225A=	GRCh37
NC_000012.10:g.13605492A=	NCBI36
NG_031854.1:g.423798T=
NG_031854.2:g.425722T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1492T= MANE Select	ENSP00000477455.1:n.*1492T=
ENST00000637214.1:c.69+47312T=	ENSP00000489997.1:n.69+47312T=
ENST00000609686.3:c.*1492T=	ENSP00000477455.1:n.*1492T=
XM_005253351.2:c.*1492T=	XP_005253408.1:n.*1492T=
XM_011520628.1:c.*1492T=	XP_011518930.1:n.*1492T=
XM_011520629.1:c.*1492T=	XP_011518931.1:n.*1492T=
XM_011520630.1:c.*1492T=	XP_011518932.1:n.*1492T=
NM_000834.4:c.*1492T=	NP_000825.2:n.*1492T=
XM_005253351.3:c.*1492T=	XP_005253408.1:n.*1492T=
XM_011520628.2:c.*1492T=	XP_011518930.1:n.*1492T=
XM_011520629.2:c.*1492T=	XP_011518931.1:n.*1492T=
XM_017019219.2:c.*1492T=	XP_016874708.1:n.*1492T=
NM_000834.5:c.*1492T= MANE Select	NP_000825.2:n.*1492T=