Canonical Allele Identifier: CA685661390

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1491512583
• MyVariant Identifiers: chr12:g.13715236_13715237del (hg19) ; chr12:g.13562302_13562303del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562303_13562304del , CM000674.2:g.13562303_13562304del	GRCh38
NC_000012.11:g.13715237_13715238del , CM000674.1:g.13715237_13715238del	GRCh37
NC_000012.10:g.13606504_13606505del	NCBI36
NG_031854.1:g.422786_422787del
NG_031854.2:g.424710_424711del

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*480_*481del MANE Select	ENSP00000477455.1:n.*480_*481del
ENST00000637214.1:c.69+46300_69+46301del	ENSP00000489997.1:n.69+46300_69+46301del
ENST00000609686.3:c.*480_*481del	ENSP00000477455.1:n.*480_*481del
NM_000834.3:c.*480_*481del	NP_000825.2:n.*480_*481del
XM_005253351.2:c.*480_*481del	XP_005253408.1:n.*480_*481del
XM_011520628.1:c.*480_*481del	XP_011518930.1:n.*480_*481del
XM_011520629.1:c.*480_*481del	XP_011518931.1:n.*480_*481del
XM_011520630.1:c.*480_*481del	XP_011518932.1:n.*480_*481del
NM_000834.4:c.*480_*481del	NP_000825.2:n.*480_*481del
XM_005253351.3:c.*480_*481del	XP_005253408.1:n.*480_*481del
XM_011520628.2:c.*480_*481del	XP_011518930.1:n.*480_*481del
XM_011520629.2:c.*480_*481del	XP_011518931.1:n.*480_*481del
XM_017019219.2:c.*480_*481del	XP_016874708.1:n.*480_*481del
NM_000834.5:c.*480_*481del MANE Select	NP_000825.2:n.*480_*481del