Canonical Allele Identifier: CA2017578140

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865770G= , CM000674.2:g.13865770G=	GRCh38
NC_000012.11:g.14018704G= , CM000674.1:g.14018704G=	GRCh37
NC_000012.10:g.13909971G=	NCBI36
NG_031854.1:g.119319C=
NG_031854.2:g.121243C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.411+28C= MANE Select	ENSP00000477455.1:n.411+28C=
ENST00000630791.2:c.411+28C=	ENSP00000486677.2:n.411+28C=
ENST00000609686.3:c.411+28C=	ENSP00000477455.1:n.411+28C=
NM_000834.3:c.411+28C=	NP_000825.2:n.411+28C=
XM_011520628.1:c.411+28C=	XP_011518930.1:n.411+28C=
XM_011520629.1:c.411+28C=	XP_011518931.1:n.411+28C=
XM_011520630.1:c.411+28C=	XP_011518932.1:n.411+28C=
NM_000834.4:c.411+28C=	NP_000825.2:n.411+28C=
XM_011520628.2:c.411+28C=	XP_011518930.1:n.411+28C=
XM_011520629.2:c.411+28C=	XP_011518931.1:n.411+28C=
XM_017019219.2:c.411+28C=	XP_016874708.1:n.411+28C=
NM_000834.5:c.411+28C= MANE Select	NP_000825.2:n.411+28C=