Canonical Allele Identifier: CA944948496

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1949456050
• gnomAD v3: 12-13617199-TG-T
• gnomAD v4: 12-13617199-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13617201del , CM000674.2:g.13617201del	GRCh38
NC_000012.11:g.13770135del , CM000674.1:g.13770135del	GRCh37
NC_000012.10:g.13661402del	NCBI36
NG_031854.1:g.367889del
NG_031854.2:g.369813del

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1126-543del MANE Select	ENSP00000477455.1:n.1126-543del
ENST00000630791.2:c.1126-543del	ENSP00000486677.2:n.1126-543del
ENST00000609686.3:c.1126-543del	ENSP00000477455.1:n.1126-543del
NM_000834.3:c.1126-543del	NP_000825.2:n.1126-543del
XM_011520628.1:c.1126-543del	XP_011518930.1:n.1126-543del
XM_011520629.1:c.1126-543del	XP_011518931.1:n.1126-543del
XM_011520630.1:c.1126-543del	XP_011518932.1:n.1126-543del
XR_931372.1:n.307+1975del
XR_931373.1:n.447+1975del
XR_931374.1:n.246+1975del
NM_000834.4:c.1126-543del	NP_000825.2:n.1126-543del
XM_011520628.2:c.1126-543del	XP_011518930.1:n.1126-543del
XM_011520629.2:c.1126-543del	XP_011518931.1:n.1126-543del
XM_017019219.2:c.1126-543del	XP_016874708.1:n.1126-543del
XR_001749013.1:n.728+1975del
XR_931372.2:n.444+1975del
XR_931373.2:n.586+1975del
NM_000834.5:c.1126-543del MANE Select	NP_000825.2:n.1126-543del