Canonical Allele Identifier: CA2575085911

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865827dup , CM000674.2:g.13865827dup	GRCh38
NC_000012.11:g.14018761dup , CM000674.1:g.14018761dup	GRCh37
NC_000012.10:g.13910028dup	NCBI36
NG_031854.1:g.119266dup
NG_031854.2:g.121190dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.386dup MANE Select	ENSP00000477455.1:p.Ser130LeufsTer8
ENST00000630791.2:c.386dup	ENSP00000486677.2:p.Ser130LeufsTer8
ENST00000609686.3:c.386dup	ENSP00000477455.1:p.Ser130LeufsTer8
NM_000834.3:c.386dup	NP_000825.2:p.Ser130LeufsTer8
XM_011520628.1:c.386dup	XP_011518930.1:p.Ser130LeufsTer8
XM_011520629.1:c.386dup	XP_011518931.1:p.Ser130LeufsTer8
XM_011520630.1:c.386dup	XP_011518932.1:p.Ser130LeufsTer8
NM_000834.4:c.386dup	NP_000825.2:p.Ser130LeufsTer8
XM_011520628.2:c.386dup	XP_011518930.1:p.Ser130LeufsTer8
XM_011520629.2:c.386dup	XP_011518931.1:p.Ser130LeufsTer8
XM_017019219.2:c.386dup	XP_016874708.1:p.Ser130LeufsTer8
NM_000834.5:c.386dup MANE Select	NP_000825.2:p.Ser130LeufsTer8