Canonical Allele Identifier: CA2017437644

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562374A= , CM000674.2:g.13562374A=	GRCh38
NC_000012.11:g.13715308A= , CM000674.1:g.13715308A=	GRCh37
NC_000012.10:g.13606575A=	NCBI36
NG_031854.1:g.422715T=
NG_031854.2:g.424639T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*409T= MANE Select	ENSP00000477455.1:n.*409T=
ENST00000637214.1:c.69+46229T=	ENSP00000489997.1:n.69+46229T=
ENST00000609686.3:c.*409T=	ENSP00000477455.1:n.*409T=
NM_000834.3:c.*409T=	NP_000825.2:n.*409T=
XM_005253351.2:c.*409T=	XP_005253408.1:n.*409T=
XM_011520628.1:c.*409T=	XP_011518930.1:n.*409T=
XM_011520629.1:c.*409T=	XP_011518931.1:n.*409T=
XM_011520630.1:c.*409T=	XP_011518932.1:n.*409T=
NM_000834.4:c.*409T=	NP_000825.2:n.*409T=
XM_005253351.3:c.*409T=	XP_005253408.1:n.*409T=
XM_011520628.2:c.*409T=	XP_011518930.1:n.*409T=
XM_011520629.2:c.*409T=	XP_011518931.1:n.*409T=
XM_017019219.2:c.*409T=	XP_016874708.1:n.*409T=
NM_000834.5:c.*409T= MANE Select	NP_000825.2:n.*409T=