Canonical Allele Identifier: CA919028331

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1591643324
• gnomAD v3: 12-13962586-CA-C
• gnomAD v4: 12-13962586-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13962590del , CM000674.2:g.13962590del	GRCh38
NC_000012.11:g.14115524del , CM000674.1:g.14115524del	GRCh37
NC_000012.10:g.14006791del	NCBI36
NG_031854.1:g.22502del
NG_031854.2:g.24426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-19+17341del MANE Select	ENSP00000477455.1:n.-19+17341del
ENST00000630791.2:c.-19+17341del	ENSP00000486677.2:n.-19+17341del
ENST00000609686.3:c.-19+17341del	ENSP00000477455.1:n.-19+17341del
ENST00000627535.2:c.-19+17341del	ENSP00000486411.1:n.-19+17341del
ENST00000630791.1:c.-19+17341del	ENSP00000486677.1:n.-19+17341del
NM_000834.3:c.-19+17341del	NP_000825.2:n.-19+17341del
XM_011520628.1:c.-19+17341del	XP_011518930.1:n.-19+17341del
XM_011520629.1:c.-19+17341del	XP_011518931.1:n.-19+17341del
XM_011520630.1:c.-19+17341del	XP_011518932.1:n.-19+17341del
NM_000834.4:c.-19+17341del	NP_000825.2:n.-19+17341del
XM_011520628.2:c.-19+17341del	XP_011518930.1:n.-19+17341del
XM_011520629.2:c.-19+17341del	XP_011518931.1:n.-19+17341del
XM_017019219.2:c.-19+17341del	XP_016874708.1:n.-19+17341del
NM_000834.5:c.-19+17341del MANE Select	NP_000825.2:n.-19+17341del