Canonical Allele Identifier: CA944929814

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1948554108
• gnomAD v3: 12-13562183-TG-T
• gnomAD v4: 12-13562183-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562187del , CM000674.2:g.13562187del	GRCh38
NC_000012.11:g.13715121del , CM000674.1:g.13715121del	GRCh37
NC_000012.10:g.13606388del	NCBI36
NG_031854.1:g.422905del
NG_031854.2:g.424829del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*599del MANE Select	ENSP00000477455.1:n.*599del
ENST00000636207.1:n.54+54del
ENST00000637214.1:c.69+46419del	ENSP00000489997.1:n.69+46419del
ENST00000609686.3:c.*599del	ENSP00000477455.1:n.*599del
NM_000834.3:c.*599del	NP_000825.2:n.*599del
XM_005253351.2:c.*599del	XP_005253408.1:n.*599del
XM_011520628.1:c.*599del	XP_011518930.1:n.*599del
XM_011520629.1:c.*599del	XP_011518931.1:n.*599del
XM_011520630.1:c.*599del	XP_011518932.1:n.*599del
NM_000834.4:c.*599del	NP_000825.2:n.*599del
XM_005253351.3:c.*599del	XP_005253408.1:n.*599del
XM_011520628.2:c.*599del	XP_011518930.1:n.*599del
XM_011520629.2:c.*599del	XP_011518931.1:n.*599del
XM_017019219.2:c.*599del	XP_016874708.1:n.*599del
NM_000834.5:c.*599del MANE Select	NP_000825.2:n.*599del