Canonical Allele Identifier: CA2017437575

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1948554614

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562226_13562236del , CM000674.2:g.13562226_13562236del	GRCh38
NC_000012.11:g.13715160_13715170del , CM000674.1:g.13715160_13715170del	GRCh37
NC_000012.10:g.13606427_13606437del	NCBI36
NG_031854.1:g.422855_422865del
NG_031854.2:g.424779_424789del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*549_*559del MANE Select	ENSP00000477455.1:n.*549_*559del
ENST00000636207.1:n.54+4_54+14del
ENST00000637214.1:c.69+46369_69+46379del	ENSP00000489997.1:n.69+46369_69+46379del
ENST00000609686.3:c.*549_*559del	ENSP00000477455.1:n.*549_*559del
NM_000834.3:c.*549_*559del	NP_000825.2:n.*549_*559del
XM_005253351.2:c.*549_*559del	XP_005253408.1:n.*549_*559del
XM_011520628.1:c.*549_*559del	XP_011518930.1:n.*549_*559del
XM_011520629.1:c.*549_*559del	XP_011518931.1:n.*549_*559del
XM_011520630.1:c.*549_*559del	XP_011518932.1:n.*549_*559del
NM_000834.4:c.*549_*559del	NP_000825.2:n.*549_*559del
XM_005253351.3:c.*549_*559del	XP_005253408.1:n.*549_*559del
XM_011520628.2:c.*549_*559del	XP_011518930.1:n.*549_*559del
XM_011520629.2:c.*549_*559del	XP_011518931.1:n.*549_*559del
XM_017019219.2:c.*549_*559del	XP_016874708.1:n.*549_*559del
NM_000834.5:c.*549_*559del MANE Select	NP_000825.2:n.*549_*559del