Canonical Allele Identifier: CA2017417478

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13564038G= , CM000674.2:g.13564038G=	GRCh38
NC_000012.11:g.13716972G= , CM000674.1:g.13716972G=	GRCh37
NC_000012.10:g.13608239G=	NCBI36
NG_031854.1:g.421051C=
NG_031854.2:g.422975C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.3200C= MANE Select	ENSP00000477455.1:p.Thr1067=
ENST00000637214.1:c.69+44565C=	ENSP00000489997.1:n.69+44565C=
ENST00000609686.3:c.3200C=	ENSP00000477455.1:p.Thr1067=
ENST00000628166.1:n.1460C=
NM_000834.3:c.3200C=	NP_000825.2:p.Thr1067=
XM_005253351.2:c.986C=	XP_005253408.1:p.Thr329=
XM_011520628.1:c.3200C=	XP_011518930.1:p.Thr1067=
XM_011520629.1:c.3200C=	XP_011518931.1:p.Thr1067=
XM_011520630.1:c.3200C=	XP_011518932.1:p.Thr1067=
NM_000834.4:c.3200C=	NP_000825.2:p.Thr1067=
XM_005253351.3:c.986C=	XP_005253408.1:p.Thr329=
XM_011520628.2:c.3200C=	XP_011518930.1:p.Thr1067=
XM_011520629.2:c.3200C=	XP_011518931.1:p.Thr1067=
XM_017019219.2:c.3200C=	XP_016874708.1:p.Thr1067=
NM_000834.5:c.3200C= MANE Select	NP_000825.2:p.Thr1067=