Canonical Allele Identifier: CA2017462968

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615226G= , CM000674.2:g.13615226G=	GRCh38
NC_000012.11:g.13768160G= , CM000674.1:g.13768160G=	GRCh37
NC_000012.10:g.13659427G=	NCBI36
NG_031854.1:g.369863C=
NG_031854.2:g.371787C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1542C= MANE Select	ENSP00000477455.1:p.Thr514=
ENST00000609686.3:c.1542C=	ENSP00000477455.1:p.Thr514=
NM_000834.3:c.1542C=	NP_000825.2:p.Thr514=
XM_011520628.1:c.1542C=	XP_011518930.1:p.Thr514=
XM_011520629.1:c.1542C=	XP_011518931.1:p.Thr514=
XM_011520630.1:c.1542C=	XP_011518932.1:p.Thr514=
XR_931372.1:n.307G=
XR_931373.1:n.447G=
XR_931374.1:n.246G=
NM_000834.4:c.1542C=	NP_000825.2:p.Thr514=
XM_011520628.2:c.1542C=	XP_011518930.1:p.Thr514=
XM_011520629.2:c.1542C=	XP_011518931.1:p.Thr514=
XM_017019219.2:c.1542C=	XP_016874708.1:p.Thr514=
XR_001749013.1:n.728G=
XR_931372.2:n.444G=
XR_931373.2:n.586G=
NM_000834.5:c.1542C= MANE Select	NP_000825.2:p.Thr514=