Canonical Allele Identifier: CA2017622218

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1867714163

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13962599del , CM000674.2:g.13962599del	GRCh38
NC_000012.11:g.14115533del , CM000674.1:g.14115533del	GRCh37
NC_000012.10:g.14006800del	NCBI36
NG_031854.1:g.22492del
NG_031854.2:g.24416del

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.-19+17331del MANE Select	ENSP00000477455.1:n.-19+17331del
ENST00000630791.2:c.-19+17331del	ENSP00000486677.2:n.-19+17331del
ENST00000609686.3:c.-19+17331del	ENSP00000477455.1:n.-19+17331del
ENST00000627535.2:c.-19+17331del	ENSP00000486411.1:n.-19+17331del
ENST00000630791.1:c.-19+17331del	ENSP00000486677.1:n.-19+17331del
NM_000834.3:c.-19+17331del	NP_000825.2:n.-19+17331del
XM_011520628.1:c.-19+17331del	XP_011518930.1:n.-19+17331del
XM_011520629.1:c.-19+17331del	XP_011518931.1:n.-19+17331del
XM_011520630.1:c.-19+17331del	XP_011518932.1:n.-19+17331del
NM_000834.4:c.-19+17331del	NP_000825.2:n.-19+17331del
XM_011520628.2:c.-19+17331del	XP_011518930.1:n.-19+17331del
XM_011520629.2:c.-19+17331del	XP_011518931.1:n.-19+17331del
XM_017019219.2:c.-19+17331del	XP_016874708.1:n.-19+17331del
NM_000834.5:c.-19+17331del MANE Select	NP_000825.2:n.-19+17331del