Canonical Allele Identifier: CA944929894

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1948556478
• gnomAD v3: 12-13562382-A-AT
• gnomAD v4: 12-13562382-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562382_13562383insT , CM000674.2:g.13562382_13562383insT	GRCh38
NC_000012.11:g.13715316_13715317insT , CM000674.1:g.13715316_13715317insT	GRCh37
NC_000012.10:g.13606583_13606584insT	NCBI36
NG_031854.1:g.422706_422707insA
NG_031854.2:g.424630_424631insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*400_*401insA MANE Select	ENSP00000477455.1:n.*400_*401insA
ENST00000637214.1:c.69+46220_69+46221insA	ENSP00000489997.1:n.69+46220_69+46221insA...
ENST00000609686.3:c.*400_*401insA	ENSP00000477455.1:n.*400_*401insA
NM_000834.3:c.*400_*401insA	NP_000825.2:n.*400_*401insA
XM_005253351.2:c.*400_*401insA	XP_005253408.1:n.*400_*401insA
XM_011520628.1:c.*400_*401insA	XP_011518930.1:n.*400_*401insA
XM_011520629.1:c.*400_*401insA	XP_011518931.1:n.*400_*401insA
XM_011520630.1:c.*400_*401insA	XP_011518932.1:n.*400_*401insA
NM_000834.4:c.*400_*401insA	NP_000825.2:n.*400_*401insA
XM_005253351.3:c.*400_*401insA	XP_005253408.1:n.*400_*401insA
XM_011520628.2:c.*400_*401insA	XP_011518930.1:n.*400_*401insA
XM_011520629.2:c.*400_*401insA	XP_011518931.1:n.*400_*401insA
XM_017019219.2:c.*400_*401insA	XP_016874708.1:n.*400_*401insA
NM_000834.5:c.*400_*401insA MANE Select	NP_000825.2:n.*400_*401insA