Canonical Allele Identifier: CA944953897

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1864954493
• gnomAD v3: 12-13822301-T-TATCC
• gnomAD v4: 12-13822301-T-TATCC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13822302_13822305dup , CM000674.2:g.13822302_13822305dup	GRCh38
NC_000012.11:g.13975236_13975239dup , CM000674.1:g.13975236_13975239dup	GRCh37
NC_000012.10:g.13866503_13866506dup	NCBI36
NG_031854.1:g.162784_162787dup
NG_031854.2:g.164708_164711dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.411+43493_411+43496dup MANE Select	ENSP00000477455.1:n.411+43493_411+43496du...
ENST00000630791.2:c.411+43493_411+43496dup	ENSP00000486677.2:n.411+43493_411+43496du...
ENST00000609686.3:c.411+43493_411+43496dup	ENSP00000477455.1:n.411+43493_411+43496du...
NM_000834.3:c.411+43493_411+43496dup	NP_000825.2:n.411+43493_411+43496dup
XM_011520628.1:c.411+43493_411+43496dup	XP_011518930.1:n.411+43493_411+43496dup
XM_011520629.1:c.411+43493_411+43496dup	XP_011518931.1:n.411+43493_411+43496dup
XM_011520630.1:c.411+43493_411+43496dup	XP_011518932.1:n.411+43493_411+43496dup
NM_000834.4:c.411+43493_411+43496dup	NP_000825.2:n.411+43493_411+43496dup
XM_011520628.2:c.411+43493_411+43496dup	XP_011518930.1:n.411+43493_411+43496dup
XM_011520629.2:c.411+43493_411+43496dup	XP_011518931.1:n.411+43493_411+43496dup
XM_017019219.2:c.411+43493_411+43496dup	XP_016874708.1:n.411+43493_411+43496dup
NM_000834.5:c.411+43493_411+43496dup MANE Select	NP_000825.2:n.411+43493_411+43496dup