Canonical Allele Identifier: CA2017448148

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608993C= , CM000674.2:g.13608993C=	GRCh38
NC_000012.11:g.13761927C= , CM000674.1:g.13761927C=	GRCh37
NC_000012.10:g.13653194C=	NCBI36
NG_031854.1:g.376096G=
NG_031854.2:g.378020G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-161G= MANE Select	ENSP00000477455.1:n.1781-161G=
ENST00000628166.2:n.41-161G=
ENST00000609686.3:c.1781-161G=	ENSP00000477455.1:n.1781-161G=
ENST00000628166.1:n.41-161G=
NM_000834.3:c.1781-161G=	NP_000825.2:n.1781-161G=
XM_011520628.1:c.1781-161G=	XP_011518930.1:n.1781-161G=
XM_011520629.1:c.1781-161G=	XP_011518931.1:n.1781-161G=
XM_011520630.1:c.1781-161G=	XP_011518932.1:n.1781-161G=
XR_931372.1:n.179-6105C=
XR_931373.1:n.318+236C=
NM_000834.4:c.1781-161G=	NP_000825.2:n.1781-161G=
XM_011520628.2:c.1781-161G=	XP_011518930.1:n.1781-161G=
XM_011520629.2:c.1781-161G=	XP_011518931.1:n.1781-161G=
XM_017019219.2:c.1781-161G=	XP_016874708.1:n.1781-161G=
XR_001749013.1:n.457+236C=
XR_931372.2:n.316-6105C=
XR_931373.2:n.457+236C=
NM_000834.5:c.1781-161G= MANE Select	NP_000825.2:n.1781-161G=