Canonical Allele Identifier: CA2017447939

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608821G= , CM000674.2:g.13608821G=	GRCh38
NC_000012.11:g.13761755G= , CM000674.1:g.13761755G=	GRCh37
NC_000012.10:g.13653022G=	NCBI36
NG_031854.1:g.376268C=
NG_031854.2:g.378192C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1792C= MANE Select	ENSP00000477455.1:p.Pro598=
ENST00000628166.2:n.52C=
ENST00000609686.3:c.1792C=	ENSP00000477455.1:p.Pro598=
ENST00000628166.1:n.52C=
NM_000834.3:c.1792C=	NP_000825.2:p.Pro598=
XM_011520628.1:c.1792C=	XP_011518930.1:p.Pro598=
XM_011520629.1:c.1792C=	XP_011518931.1:p.Pro598=
XM_011520630.1:c.1792C=	XP_011518932.1:p.Pro598=
XR_931372.1:n.179-6277G=
XR_931373.1:n.318+64G=
NM_000834.4:c.1792C=	NP_000825.2:p.Pro598=
XM_011520628.2:c.1792C=	XP_011518930.1:p.Pro598=
XM_011520629.2:c.1792C=	XP_011518931.1:p.Pro598=
XM_017019219.2:c.1792C=	XP_016874708.1:p.Pro598=
XR_001749013.1:n.457+64G=
XR_931372.2:n.316-6277G=
XR_931373.2:n.457+64G=
NM_000834.5:c.1792C= MANE Select	NP_000825.2:p.Pro598=