Canonical Allele Identifier: CA2617718165

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13562254-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562256dup , CM000674.2:g.13562256dup	GRCh38
NC_000012.11:g.13715190dup , CM000674.1:g.13715190dup	GRCh37
NC_000012.10:g.13606457dup	NCBI36
NG_031854.1:g.422834dup
NG_031854.2:g.424758dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*528dup MANE Select	ENSP00000477455.1:n.*528dup
ENST00000636207.1:n.37dup
ENST00000637214.1:c.69+46348dup	ENSP00000489997.1:n.69+46348dup
ENST00000609686.3:c.*528dup	ENSP00000477455.1:n.*528dup
NM_000834.3:c.*528dup	NP_000825.2:n.*528dup
XM_005253351.2:c.*528dup	XP_005253408.1:n.*528dup
XM_011520628.1:c.*528dup	XP_011518930.1:n.*528dup
XM_011520629.1:c.*528dup	XP_011518931.1:n.*528dup
XM_011520630.1:c.*528dup	XP_011518932.1:n.*528dup
NM_000834.4:c.*528dup	NP_000825.2:n.*528dup
XM_005253351.3:c.*528dup	XP_005253408.1:n.*528dup
XM_011520628.2:c.*528dup	XP_011518930.1:n.*528dup
XM_011520629.2:c.*528dup	XP_011518931.1:n.*528dup
XM_017019219.2:c.*528dup	XP_016874708.1:n.*528dup
NM_000834.5:c.*528dup MANE Select	NP_000825.2:n.*528dup