Canonical Allele Identifier: CA2017414831

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13563130C= , CM000674.2:g.13563130C=	GRCh38
NC_000012.11:g.13716064C= , CM000674.1:g.13716064C=	GRCh37
NC_000012.10:g.13607331C=	NCBI36
NG_031854.1:g.421959G=
NG_031854.2:g.423883G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.4108G= MANE Select	ENSP00000477455.1:p.Gly1370=
ENST00000637214.1:c.69+45473G=	ENSP00000489997.1:n.69+45473G=
ENST00000609686.3:c.4108G=	ENSP00000477455.1:p.Gly1370=
ENST00000628166.1:n.2368G=
NM_000834.3:c.4108G=	NP_000825.2:p.Gly1370=
XM_005253351.2:c.1894G=	XP_005253408.1:p.Gly632=
XM_011520628.1:c.4108G=	XP_011518930.1:p.Gly1370=
XM_011520629.1:c.4108G=	XP_011518931.1:p.Gly1370=
XM_011520630.1:c.4108G=	XP_011518932.1:p.Gly1370=
NM_000834.4:c.4108G=	NP_000825.2:p.Gly1370=
XM_005253351.3:c.1894G=	XP_005253408.1:p.Gly632=
XM_011520628.2:c.4108G=	XP_011518930.1:p.Gly1370=
XM_011520629.2:c.4108G=	XP_011518931.1:p.Gly1370=
XM_017019219.2:c.4108G=	XP_016874708.1:p.Gly1370=
NM_000834.5:c.4108G= MANE Select	NP_000825.2:p.Gly1370=