Canonical Allele Identifier: CA2017437182

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1948542918

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561491_13561493del , CM000674.2:g.13561491_13561493del	GRCh38
NC_000012.11:g.13714425_13714427del , CM000674.1:g.13714425_13714427del	GRCh37
NC_000012.10:g.13605692_13605694del	NCBI36
NG_031854.1:g.423600_423602del
NG_031854.2:g.425524_425526del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1294_*1296del MANE Select	ENSP00000477455.1:n.*1294_*1296del
ENST00000637214.1:c.69+47114_69+47116del	ENSP00000489997.1:n.69+47114_69+47116del
ENST00000609686.3:c.*1294_*1296del	ENSP00000477455.1:n.*1294_*1296del
NM_000834.3:c.*1294_*1296del	NP_000825.2:n.*1294_*1296del
XM_005253351.2:c.*1294_*1296del	XP_005253408.1:n.*1294_*1296del
XM_011520628.1:c.*1294_*1296del	XP_011518930.1:n.*1294_*1296del
XM_011520629.1:c.*1294_*1296del	XP_011518931.1:n.*1294_*1296del
XM_011520630.1:c.*1294_*1296del	XP_011518932.1:n.*1294_*1296del
NM_000834.4:c.*1294_*1296del	NP_000825.2:n.*1294_*1296del
XM_005253351.3:c.*1294_*1296del	XP_005253408.1:n.*1294_*1296del
XM_011520628.2:c.*1294_*1296del	XP_011518930.1:n.*1294_*1296del
XM_011520629.2:c.*1294_*1296del	XP_011518931.1:n.*1294_*1296del
XM_017019219.2:c.*1294_*1296del	XP_016874708.1:n.*1294_*1296del
NM_000834.5:c.*1294_*1296del MANE Select	NP_000825.2:n.*1294_*1296del