Canonical Allele Identifier: CA2017450740

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611795T= , CM000674.2:g.13611795T=	GRCh38
NC_000012.11:g.13764729T= , CM000674.1:g.13764729T=	GRCh37
NC_000012.10:g.13655996T=	NCBI36
NG_031854.1:g.373294A=
NG_031854.2:g.375218A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1710A= MANE Select	ENSP00000477455.1:p.Ser570=
ENST00000609686.3:c.1710A=	ENSP00000477455.1:p.Ser570=
NM_000834.3:c.1710A=	NP_000825.2:p.Ser570=
XM_011520628.1:c.1710A=	XP_011518930.1:p.Ser570=
XM_011520629.1:c.1710A=	XP_011518931.1:p.Ser570=
XM_011520630.1:c.1710A=	XP_011518932.1:p.Ser570=
XR_931372.1:n.179-3303T=
XR_931373.1:n.318+3038T=
XR_931374.1:n.117+1195T=
NM_000834.4:c.1710A=	NP_000825.2:p.Ser570=
XM_011520628.2:c.1710A=	XP_011518930.1:p.Ser570=
XM_011520629.2:c.1710A=	XP_011518931.1:p.Ser570=
XM_017019219.2:c.1710A=	XP_016874708.1:p.Ser570=
XR_001749013.1:n.599+1195T=
XR_931372.2:n.316-3303T=
XR_931373.2:n.457+3038T=
NM_000834.5:c.1710A= MANE Select	NP_000825.2:p.Ser570=