Canonical Allele Identifier: CA2617717870

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13561481-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561487dup , CM000674.2:g.13561487dup	GRCh38
NC_000012.11:g.13714421dup , CM000674.1:g.13714421dup	GRCh37
NC_000012.10:g.13605688dup	NCBI36
NG_031854.1:g.423607dup
NG_031854.2:g.425531dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1301dup MANE Select	ENSP00000477455.1:n.*1301dup
ENST00000637214.1:c.69+47121dup	ENSP00000489997.1:n.69+47121dup
ENST00000609686.3:c.*1301dup	ENSP00000477455.1:n.*1301dup
NM_000834.3:c.*1301dup	NP_000825.2:n.*1301dup
XM_005253351.2:c.*1301dup	XP_005253408.1:n.*1301dup
XM_011520628.1:c.*1301dup	XP_011518930.1:n.*1301dup
XM_011520629.1:c.*1301dup	XP_011518931.1:n.*1301dup
XM_011520630.1:c.*1301dup	XP_011518932.1:n.*1301dup
NM_000834.4:c.*1301dup	NP_000825.2:n.*1301dup
XM_005253351.3:c.*1301dup	XP_005253408.1:n.*1301dup
XM_011520628.2:c.*1301dup	XP_011518930.1:n.*1301dup
XM_011520629.2:c.*1301dup	XP_011518931.1:n.*1301dup
XM_017019219.2:c.*1301dup	XP_016874708.1:n.*1301dup
NM_000834.5:c.*1301dup MANE Select	NP_000825.2:n.*1301dup