Canonical Allele Identifier: CA2017418147

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13564263T= , CM000674.2:g.13564263T=	GRCh38
NC_000012.11:g.13717197T= , CM000674.1:g.13717197T=	GRCh37
NC_000012.10:g.13608464T=	NCBI36
NG_031854.1:g.420826A=
NG_031854.2:g.422750A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.2975A= MANE Select	ENSP00000477455.1:p.His992=
ENST00000637214.1:c.69+44340A=	ENSP00000489997.1:n.69+44340A=
ENST00000609686.3:c.2975A=	ENSP00000477455.1:p.His992=
ENST00000628166.1:n.1235A=
NM_000834.3:c.2975A=	NP_000825.2:p.His992=
XM_005253351.2:c.761A=	XP_005253408.1:p.His254=
XM_011520628.1:c.2975A=	XP_011518930.1:p.His992=
XM_011520629.1:c.2975A=	XP_011518931.1:p.His992=
XM_011520630.1:c.2975A=	XP_011518932.1:p.His992=
NM_000834.4:c.2975A=	NP_000825.2:p.His992=
XM_005253351.3:c.761A=	XP_005253408.1:p.His254=
XM_011520628.2:c.2975A=	XP_011518930.1:p.His992=
XM_011520629.2:c.2975A=	XP_011518931.1:p.His992=
XM_017019219.2:c.2975A=	XP_016874708.1:p.His992=
NM_000834.5:c.2975A= MANE Select	NP_000825.2:p.His992=