Canonical Allele Identifier: CA2017440434

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13569836C= , CM000674.2:g.13569836C=	GRCh38
NC_000012.11:g.13722770C= , CM000674.1:g.13722770C=	GRCh37
NC_000012.10:g.13614037C=	NCBI36
NG_031854.1:g.415253G=
NG_031854.2:g.417177G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.2353G= MANE Select	ENSP00000477455.1:p.Gly785=
ENST00000628166.2:n.613G=
ENST00000637214.1:c.69+38767G=	ENSP00000489997.1:n.69+38767G=
ENST00000609686.3:c.2353G=	ENSP00000477455.1:p.Gly785=
ENST00000628166.1:n.613G=
NM_000834.3:c.2353G=	NP_000825.2:p.Gly785=
XM_005253351.2:c.139G=	XP_005253408.1:p.Gly47=
XM_011520628.1:c.2353G=	XP_011518930.1:p.Gly785=
XM_011520629.1:c.2353G=	XP_011518931.1:p.Gly785=
XM_011520630.1:c.2353G=	XP_011518932.1:p.Gly785=
NM_000834.4:c.2353G=	NP_000825.2:p.Gly785=
XM_005253351.3:c.139G=	XP_005253408.1:p.Gly47=
XM_011520628.2:c.2353G=	XP_011518930.1:p.Gly785=
XM_011520629.2:c.2353G=	XP_011518931.1:p.Gly785=
XM_017019219.2:c.2353G=	XP_016874708.1:p.Gly785=
NM_000834.5:c.2353G= MANE Select	NP_000825.2:p.Gly785=