Canonical Allele Identifier: CA2017448083

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608926A= , CM000674.2:g.13608926A=	GRCh38
NC_000012.11:g.13761860A= , CM000674.1:g.13761860A=	GRCh37
NC_000012.10:g.13653127A=	NCBI36
NG_031854.1:g.376163T=
NG_031854.2:g.378087T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-94T= MANE Select	ENSP00000477455.1:n.1781-94T=
ENST00000628166.2:n.41-94T=
ENST00000609686.3:c.1781-94T=	ENSP00000477455.1:n.1781-94T=
ENST00000628166.1:n.41-94T=
NM_000834.3:c.1781-94T=	NP_000825.2:n.1781-94T=
XM_011520628.1:c.1781-94T=	XP_011518930.1:n.1781-94T=
XM_011520629.1:c.1781-94T=	XP_011518931.1:n.1781-94T=
XM_011520630.1:c.1781-94T=	XP_011518932.1:n.1781-94T=
XR_931372.1:n.179-6172A=
XR_931373.1:n.318+169A=
NM_000834.4:c.1781-94T=	NP_000825.2:n.1781-94T=
XM_011520628.2:c.1781-94T=	XP_011518930.1:n.1781-94T=
XM_011520629.2:c.1781-94T=	XP_011518931.1:n.1781-94T=
XM_017019219.2:c.1781-94T=	XP_016874708.1:n.1781-94T=
XR_001749013.1:n.457+169A=
XR_931372.2:n.316-6172A=
XR_931373.2:n.457+169A=
NM_000834.5:c.1781-94T= MANE Select	NP_000825.2:n.1781-94T=