Canonical Allele Identifier: CA233147996

Gene: GRIN2B

Linked Data

• dbSNP Id: rs34025626

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865778dup , CM000674.2:g.13865778dup	GRCh38
NC_000012.11:g.14018712dup , CM000674.1:g.14018712dup	GRCh37
NC_000012.10:g.13909979dup	NCBI36
NG_031854.1:g.119311dup
NG_031854.2:g.121235dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.411+20dup MANE Select	ENSP00000477455.1:n.411+20dup
ENST00000630791.2:c.411+20dup	ENSP00000486677.2:n.411+20dup
ENST00000609686.3:c.411+20dup	ENSP00000477455.1:n.411+20dup
NM_000834.3:c.411+20dup	NP_000825.2:n.411+20dup
XM_011520628.1:c.411+20dup	XP_011518930.1:n.411+20dup
XM_011520629.1:c.411+20dup	XP_011518931.1:n.411+20dup
XM_011520630.1:c.411+20dup	XP_011518932.1:n.411+20dup
NM_000834.4:c.411+20dup	NP_000825.2:n.411+20dup
XM_011520628.2:c.411+20dup	XP_011518930.1:n.411+20dup
XM_011520629.2:c.411+20dup	XP_011518931.1:n.411+20dup
XM_017019219.2:c.411+20dup	XP_016874708.1:n.411+20dup
NM_000834.5:c.411+20dup MANE Select	NP_000825.2:n.411+20dup