Canonical Allele Identifier: CA685661580

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1372560625
• gnomAD v3: 12-13562516-TGA-T
• gnomAD v4: 12-13562516-TGA-T
• MyVariant Identifiers: chr12:g.13715451_13715452del (hg19) ; chr12:g.13562517_13562518del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562520_13562521del , CM000674.2:g.13562520_13562521del	GRCh38
NC_000012.11:g.13715454_13715455del , CM000674.1:g.13715454_13715455del	GRCh37
NC_000012.10:g.13606721_13606722del	NCBI36
NG_031854.1:g.422571_422572del
NG_031854.2:g.424495_424496del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*265_*266del MANE Select	ENSP00000477455.1:n.*265_*266del
ENST00000637214.1:c.69+46085_69+46086del	ENSP00000489997.1:n.69+46085_69+46086del
ENST00000609686.3:c.*265_*266del	ENSP00000477455.1:n.*265_*266del
NM_000834.3:c.*265_*266del	NP_000825.2:n.*265_*266del
XM_005253351.2:c.*265_*266del	XP_005253408.1:n.*265_*266del
XM_011520628.1:c.*265_*266del	XP_011518930.1:n.*265_*266del
XM_011520629.1:c.*265_*266del	XP_011518931.1:n.*265_*266del
XM_011520630.1:c.*265_*266del	XP_011518932.1:n.*265_*266del
NM_000834.4:c.*265_*266del	NP_000825.2:n.*265_*266del
XM_005253351.3:c.*265_*266del	XP_005253408.1:n.*265_*266del
XM_011520628.2:c.*265_*266del	XP_011518930.1:n.*265_*266del
XM_011520629.2:c.*265_*266del	XP_011518931.1:n.*265_*266del
XM_017019219.2:c.*265_*266del	XP_016874708.1:n.*265_*266del
NM_000834.5:c.*265_*266del MANE Select	NP_000825.2:n.*265_*266del