Canonical Allele Identifier: CA2017447733

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608676T= , CM000674.2:g.13608676T=	GRCh38
NC_000012.11:g.13761610T= , CM000674.1:g.13761610T=	GRCh37
NC_000012.10:g.13652877T=	NCBI36
NG_031854.1:g.376413A=
NG_031854.2:g.378337A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1937A= MANE Select	ENSP00000477455.1:p.Tyr646=
ENST00000628166.2:n.197A=
ENST00000609686.3:c.1937A=	ENSP00000477455.1:p.Tyr646=
ENST00000628166.1:n.197A=
NM_000834.3:c.1937A=	NP_000825.2:p.Tyr646=
XM_011520628.1:c.1937A=	XP_011518930.1:p.Tyr646=
XM_011520629.1:c.1937A=	XP_011518931.1:p.Tyr646=
XM_011520630.1:c.1937A=	XP_011518932.1:p.Tyr646=
XR_931372.1:n.179-6422T=
XR_931373.1:n.237T=
NM_000834.4:c.1937A=	NP_000825.2:p.Tyr646=
XM_005253351.3:c.-117A=	XP_005253408.1:n.-117A=
XM_011520628.2:c.1937A=	XP_011518930.1:p.Tyr646=
XM_011520629.2:c.1937A=	XP_011518931.1:p.Tyr646=
XM_017019219.2:c.1937A=	XP_016874708.1:p.Tyr646=
XR_001749013.1:n.376T=
XR_931372.2:n.316-6422T=
XR_931373.2:n.376T=
NM_000834.5:c.1937A= MANE Select	NP_000825.2:p.Tyr646=