Canonical Allele Identifier: CA2017441398

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13571859T= , CM000674.2:g.13571859T=	GRCh38
NC_000012.11:g.13724793T= , CM000674.1:g.13724793T=	GRCh37
NC_000012.10:g.13616060T=	NCBI36
NG_031854.1:g.413230A=
NG_031854.2:g.415154A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000834.5:c.2116A= MANE Select	NP_000825.2:p.Met706=
ENST00000609686.4:c.2116A= MANE Select	ENSP00000477455.1:p.Met706=
NM_000834.3:c.2116A=	NP_000825.2:p.Met706=
NM_000834.4:c.2116A=	NP_000825.2:p.Met706=
ENST00000609686.3:c.2116A=	ENSP00000477455.1:p.Met706=
ENST00000628166.1:n.376A=
ENST00000628166.2:n.376A=
ENST00000637214.1:c.69+36744A=	ENSP00000489997.1:n.69+36744A=
XM_005253351.2:c.-43-1842A=	XP_005253408.1:n.-43-1842A=
XM_005253351.3:c.-43-1842A=	XP_005253408.1:n.-43-1842A=
XM_011520628.1:c.2116A=	XP_011518930.1:p.Met706=
XM_011520628.2:c.2116A=	XP_011518930.1:p.Met706=
XM_011520629.1:c.2116A=	XP_011518931.1:p.Met706=
XM_011520629.2:c.2116A=	XP_011518931.1:p.Met706=
XM_011520630.1:c.2116A=	XP_011518932.1:p.Met706=
XM_017019219.2:c.2116A=	XP_016874708.1:p.Met706=