Canonical Allele Identifier: CA2017437128

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1948541525

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561403_13561410del , CM000674.2:g.13561403_13561410del	GRCh38
NC_000012.11:g.13714337_13714344del , CM000674.1:g.13714337_13714344del	GRCh37
NC_000012.10:g.13605604_13605611del	NCBI36
NG_031854.1:g.423679_423686del
NG_031854.2:g.425603_425610del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1373_*1380del MANE Select	ENSP00000477455.1:n.*1373_*1380del
ENST00000637214.1:c.69+47193_69+47200del	ENSP00000489997.1:n.69+47193_69+47200del
ENST00000609686.3:c.*1373_*1380del	ENSP00000477455.1:n.*1373_*1380del
XM_005253351.2:c.*1373_*1380del	XP_005253408.1:n.*1373_*1380del
XM_011520628.1:c.*1373_*1380del	XP_011518930.1:n.*1373_*1380del
XM_011520629.1:c.*1373_*1380del	XP_011518931.1:n.*1373_*1380del
XM_011520630.1:c.*1373_*1380del	XP_011518932.1:n.*1373_*1380del
NM_000834.4:c.*1373_*1380del	NP_000825.2:n.*1373_*1380del
XM_005253351.3:c.*1373_*1380del	XP_005253408.1:n.*1373_*1380del
XM_011520628.2:c.*1373_*1380del	XP_011518930.1:n.*1373_*1380del
XM_011520629.2:c.*1373_*1380del	XP_011518931.1:n.*1373_*1380del
XM_017019219.2:c.*1373_*1380del	XP_016874708.1:n.*1373_*1380del
NM_000834.5:c.*1373_*1380del MANE Select	NP_000825.2:n.*1373_*1380del