Canonical Allele Identifier: CA2017441404

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13571891A= , CM000674.2:g.13571891A=	GRCh38
NC_000012.11:g.13724825A= , CM000674.1:g.13724825A=	GRCh37
NC_000012.10:g.13616092A=	NCBI36
NG_031854.1:g.413198T=
NG_031854.2:g.415122T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000834.5:c.2084T= MANE Select	NP_000825.2:p.Ile695=
ENST00000609686.4:c.2084T= MANE Select	ENSP00000477455.1:p.Ile695=
NM_000834.3:c.2084T=	NP_000825.2:p.Ile695=
NM_000834.4:c.2084T=	NP_000825.2:p.Ile695=
ENST00000609686.3:c.2084T=	ENSP00000477455.1:p.Ile695=
ENST00000628166.1:n.344T=
ENST00000628166.2:n.344T=
ENST00000637214.1:c.69+36712T=	ENSP00000489997.1:n.69+36712T=
XM_005253351.2:c.-43-1874T=	XP_005253408.1:n.-43-1874T=
XM_005253351.3:c.-43-1874T=	XP_005253408.1:n.-43-1874T=
XM_011520628.1:c.2084T=	XP_011518930.1:p.Ile695=
XM_011520628.2:c.2084T=	XP_011518930.1:p.Ile695=
XM_011520629.1:c.2084T=	XP_011518931.1:p.Ile695=
XM_011520629.2:c.2084T=	XP_011518931.1:p.Ile695=
XM_011520630.1:c.2084T=	XP_011518932.1:p.Ile695=
XM_017019219.2:c.2084T=	XP_016874708.1:p.Ile695=