Canonical Allele Identifier: CA2017440469

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13569942C= , CM000674.2:g.13569942C=	GRCh38
NC_000012.11:g.13722876C= , CM000674.1:g.13722876C=	GRCh37
NC_000012.10:g.13614143C=	NCBI36
NG_031854.1:g.415147G=
NG_031854.2:g.417071G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.2247G= MANE Select	ENSP00000477455.1:p.Val749=
ENST00000628166.2:n.507G=
ENST00000637214.1:c.69+38661G=	ENSP00000489997.1:n.69+38661G=
ENST00000609686.3:c.2247G=	ENSP00000477455.1:p.Val749=
ENST00000628166.1:n.507G=
NM_000834.3:c.2247G=	NP_000825.2:p.Val749=
XM_005253351.2:c.33G=	XP_005253408.1:p.Val11=
XM_011520628.1:c.2247G=	XP_011518930.1:p.Val749=
XM_011520629.1:c.2247G=	XP_011518931.1:p.Val749=
XM_011520630.1:c.2247G=	XP_011518932.1:p.Val749=
NM_000834.4:c.2247G=	NP_000825.2:p.Val749=
XM_005253351.3:c.33G=	XP_005253408.1:p.Val11=
XM_011520628.2:c.2247G=	XP_011518930.1:p.Val749=
XM_011520629.2:c.2247G=	XP_011518931.1:p.Val749=
XM_017019219.2:c.2247G=	XP_016874708.1:p.Val749=
NM_000834.5:c.2247G= MANE Select	NP_000825.2:p.Val749=