Canonical Allele Identifier: CA2617717669

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13561181-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561185del , CM000674.2:g.13561185del	GRCh38
NC_000012.11:g.13714119del , CM000674.1:g.13714119del	GRCh37
NC_000012.10:g.13605386del	NCBI36
NG_031854.1:g.423907del
NG_031854.2:g.425831del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1601del MANE Select	ENSP00000477455.1:n.*1601del
ENST00000637214.1:c.69+47421del	ENSP00000489997.1:n.69+47421del
ENST00000609686.3:c.*1601del	ENSP00000477455.1:n.*1601del
XM_005253351.2:c.*1601del	XP_005253408.1:n.*1601del
XM_011520628.1:c.*1601del	XP_011518930.1:n.*1601del
XM_011520629.1:c.*1601del	XP_011518931.1:n.*1601del
XM_011520630.1:c.*1601del	XP_011518932.1:n.*1601del
NM_000834.4:c.*1601del	NP_000825.2:n.*1601del
XM_005253351.3:c.*1601del	XP_005253408.1:n.*1601del
XM_011520628.2:c.*1601del	XP_011518930.1:n.*1601del
XM_011520629.2:c.*1601del	XP_011518931.1:n.*1601del
XM_017019219.2:c.*1601del	XP_016874708.1:n.*1601del
NM_000834.5:c.*1601del MANE Select	NP_000825.2:n.*1601del