Canonical Allele Identifier: CA2017438744

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13566432G= , CM000674.2:g.13566432G=	GRCh38
NC_000012.11:g.13719366G= , CM000674.1:g.13719366G=	GRCh37
NC_000012.10:g.13610633G=	NCBI36
NG_031854.1:g.418657C=
NG_031854.2:g.420581C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.2598+593C= MANE Select	ENSP00000477455.1:n.2598+593C=
ENST00000637214.1:c.69+42171C=	ENSP00000489997.1:n.69+42171C=
ENST00000609686.3:c.2598+593C=	ENSP00000477455.1:n.2598+593C=
ENST00000628166.1:n.858+593C=
NM_000834.3:c.2598+593C=	NP_000825.2:n.2598+593C=
XM_005253351.2:c.384+593C=	XP_005253408.1:n.384+593C=
XM_011520628.1:c.2598+593C=	XP_011518930.1:n.2598+593C=
XM_011520629.1:c.2598+593C=	XP_011518931.1:n.2598+593C=
XM_011520630.1:c.2598+593C=	XP_011518932.1:n.2598+593C=
NM_000834.4:c.2598+593C=	NP_000825.2:n.2598+593C=
XM_005253351.3:c.384+593C=	XP_005253408.1:n.384+593C=
XM_011520628.2:c.2598+593C=	XP_011518930.1:n.2598+593C=
XM_011520629.2:c.2598+593C=	XP_011518931.1:n.2598+593C=
XM_017019219.2:c.2598+593C=	XP_016874708.1:n.2598+593C=
NM_000834.5:c.2598+593C= MANE Select	NP_000825.2:n.2598+593C=