Canonical Allele Identifier: CA2017436976

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561142G= , CM000674.2:g.13561142G=	GRCh38
NC_000012.11:g.13714076G= , CM000674.1:g.13714076G=	GRCh37
NC_000012.10:g.13605343G=	NCBI36
NG_031854.1:g.423947C=
NG_031854.2:g.425871C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*1641C= MANE Select	ENSP00000477455.1:n.*1641C=
ENST00000637214.1:c.69+47461C=	ENSP00000489997.1:n.69+47461C=
ENST00000609686.3:c.*1641C=	ENSP00000477455.1:n.*1641C=
XM_005253351.2:c.*1641C=	XP_005253408.1:n.*1641C=
XM_011520628.1:c.*1641C=	XP_011518930.1:n.*1641C=
XM_011520629.1:c.*1641C=	XP_011518931.1:n.*1641C=
XM_011520630.1:c.*1641C=	XP_011518932.1:n.*1641C=
NM_000834.4:c.*1641C=	NP_000825.2:n.*1641C=
XM_005253351.3:c.*1641C=	XP_005253408.1:n.*1641C=
XM_011520628.2:c.*1641C=	XP_011518930.1:n.*1641C=
XM_011520629.2:c.*1641C=	XP_011518931.1:n.*1641C=
XM_017019219.2:c.*1641C=	XP_016874708.1:n.*1641C=
NM_000834.5:c.*1641C= MANE Select	NP_000825.2:n.*1641C=