Canonical Allele Identifier: CA603378204

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1264569966
• gnomAD v2: 12-13715497-C-CG
• gnomAD v3: 12-13562563-C-CG
• gnomAD v4: 12-13562563-C-CG
• MyVariant Identifiers: chr12:g.13715497_13715498insG (hg19) ; chr12:g.13562563_13562564insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562569dup , CM000674.2:g.13562569dup	GRCh38
NC_000012.11:g.13715503dup , CM000674.1:g.13715503dup	GRCh37
NC_000012.10:g.13606770dup	NCBI36
NG_031854.1:g.422525dup
NG_031854.2:g.424449dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*219dup MANE Select	ENSP00000477455.1:n.*219dup
ENST00000637214.1:c.69+46039dup	ENSP00000489997.1:n.69+46039dup
ENST00000609686.3:c.*219dup	ENSP00000477455.1:n.*219dup
NM_000834.3:c.*219dup	NP_000825.2:n.*219dup
XM_005253351.2:c.*219dup	XP_005253408.1:n.*219dup
XM_011520628.1:c.*219dup	XP_011518930.1:n.*219dup
XM_011520629.1:c.*219dup	XP_011518931.1:n.*219dup
XM_011520630.1:c.*219dup	XP_011518932.1:n.*219dup
NM_000834.4:c.*219dup	NP_000825.2:n.*219dup
XM_005253351.3:c.*219dup	XP_005253408.1:n.*219dup
XM_011520628.2:c.*219dup	XP_011518930.1:n.*219dup
XM_011520629.2:c.*219dup	XP_011518931.1:n.*219dup
XM_017019219.2:c.*219dup	XP_016874708.1:n.*219dup
NM_000834.5:c.*219dup MANE Select	NP_000825.2:n.*219dup