Canonical Allele Identifier: CA2017525999

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753898G= , CM000674.2:g.13753898G=	GRCh38
NC_000012.11:g.13906832G= , CM000674.1:g.13906832G=	GRCh37
NC_000012.10:g.13798099G=	NCBI36
NG_031854.1:g.231191C=
NG_031854.2:g.233115C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.429C= MANE Select	ENSP00000477455.1:p.Phe143=
ENST00000630791.2:c.429C=	ENSP00000486677.2:p.Phe143=
ENST00000609686.3:c.429C=	ENSP00000477455.1:p.Phe143=
NM_000834.3:c.429C=	NP_000825.2:p.Phe143=
XM_011520628.1:c.429C=	XP_011518930.1:p.Phe143=
XM_011520629.1:c.429C=	XP_011518931.1:p.Phe143=
XM_011520630.1:c.429C=	XP_011518932.1:p.Phe143=
NM_000834.4:c.429C=	NP_000825.2:p.Phe143=
XM_011520628.2:c.429C=	XP_011518930.1:p.Phe143=
XM_011520629.2:c.429C=	XP_011518931.1:p.Phe143=
XM_017019219.2:c.429C=	XP_016874708.1:p.Phe143=
NM_000834.5:c.429C= MANE Select	NP_000825.2:p.Phe143=