Canonical Allele Identifier: CA685660743

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1167615295
• MyVariant Identifiers: chr12:g.13714384_13714387del (hg19) ; chr12:g.13561450_13561453del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561453_13561456del , CM000674.2:g.13561453_13561456del	GRCh38
NC_000012.11:g.13714387_13714390del , CM000674.1:g.13714387_13714390del	GRCh37
NC_000012.10:g.13605654_13605657del	NCBI36
NG_031854.1:g.423636_423639del
NG_031854.2:g.425560_425563del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1330_*1333del MANE Select	ENSP00000477455.1:n.*1330_*1333del
ENST00000637214.1:c.69+47150_69+47153del	ENSP00000489997.1:n.69+47150_69+47153del
ENST00000609686.3:c.*1330_*1333del	ENSP00000477455.1:n.*1330_*1333del
XM_005253351.2:c.*1330_*1333del	XP_005253408.1:n.*1330_*1333del
XM_011520628.1:c.*1330_*1333del	XP_011518930.1:n.*1330_*1333del
XM_011520629.1:c.*1330_*1333del	XP_011518931.1:n.*1330_*1333del
XM_011520630.1:c.*1330_*1333del	XP_011518932.1:n.*1330_*1333del
NM_000834.4:c.*1330_*1333del	NP_000825.2:n.*1330_*1333del
XM_005253351.3:c.*1330_*1333del	XP_005253408.1:n.*1330_*1333del
XM_011520628.2:c.*1330_*1333del	XP_011518930.1:n.*1330_*1333del
XM_011520629.2:c.*1330_*1333del	XP_011518931.1:n.*1330_*1333del
XM_017019219.2:c.*1330_*1333del	XP_016874708.1:n.*1330_*1333del
NM_000834.5:c.*1330_*1333del MANE Select	NP_000825.2:n.*1330_*1333del