Canonical Allele Identifier: CA944948589

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1949458056
• gnomAD v3: 12-13617327-GC-G
• gnomAD v4: 12-13617327-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13617330del , CM000674.2:g.13617330del	GRCh38
NC_000012.11:g.13770264del , CM000674.1:g.13770264del	GRCh37
NC_000012.10:g.13661531del	NCBI36
NG_031854.1:g.367761del
NG_031854.2:g.369685del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1126-671del MANE Select	ENSP00000477455.1:n.1126-671del
ENST00000630791.2:c.1126-671del	ENSP00000486677.2:n.1126-671del
ENST00000609686.3:c.1126-671del	ENSP00000477455.1:n.1126-671del
NM_000834.3:c.1126-671del	NP_000825.2:n.1126-671del
XM_011520628.1:c.1126-671del	XP_011518930.1:n.1126-671del
XM_011520629.1:c.1126-671del	XP_011518931.1:n.1126-671del
XM_011520630.1:c.1126-671del	XP_011518932.1:n.1126-671del
XR_931372.1:n.307+2104del
XR_931373.1:n.447+2104del
XR_931374.1:n.246+2104del
NM_000834.4:c.1126-671del	NP_000825.2:n.1126-671del
XM_011520628.2:c.1126-671del	XP_011518930.1:n.1126-671del
XM_011520629.2:c.1126-671del	XP_011518931.1:n.1126-671del
XM_017019219.2:c.1126-671del	XP_016874708.1:n.1126-671del
XR_001749013.1:n.728+2104del
XR_931372.2:n.444+2104del
XR_931373.2:n.586+2104del
NM_000834.5:c.1126-671del MANE Select	NP_000825.2:n.1126-671del