Canonical Allele Identifier: CA2725499027

Gene: GRIN2B

Linked Data

• dbSNP Id: rs2136401384

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562337_13562358del , CM000674.2:g.13562337_13562358del	GRCh38
NC_000012.11:g.13715271_13715292del , CM000674.1:g.13715271_13715292del	GRCh37
NC_000012.10:g.13606538_13606559del	NCBI36
NG_031854.1:g.422736_422757del
NG_031854.2:g.424660_424681del

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*430_*451del MANE Select	ENSP00000477455.1:n.*430_*451del
ENST00000637214.1:c.69+46250_69+46271del	ENSP00000489997.1:n.69+46250_69+46271del
ENST00000609686.3:c.*430_*451del	ENSP00000477455.1:n.*430_*451del
NM_000834.3:c.*430_*451del	NP_000825.2:n.*430_*451del
XM_005253351.2:c.*430_*451del	XP_005253408.1:n.*430_*451del
XM_011520628.1:c.*430_*451del	XP_011518930.1:n.*430_*451del
XM_011520629.1:c.*430_*451del	XP_011518931.1:n.*430_*451del
XM_011520630.1:c.*430_*451del	XP_011518932.1:n.*430_*451del
NM_000834.4:c.*430_*451del	NP_000825.2:n.*430_*451del
XM_005253351.3:c.*430_*451del	XP_005253408.1:n.*430_*451del
XM_011520628.2:c.*430_*451del	XP_011518930.1:n.*430_*451del
XM_011520629.2:c.*430_*451del	XP_011518931.1:n.*430_*451del
XM_017019219.2:c.*430_*451del	XP_016874708.1:n.*430_*451del
NM_000834.5:c.*430_*451del MANE Select	NP_000825.2:n.*430_*451del