Canonical Allele Identifier: CA2617718120

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13562149-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562153del , CM000674.2:g.13562153del	GRCh38
NC_000012.11:g.13715087del , CM000674.1:g.13715087del	GRCh37
NC_000012.10:g.13606354del	NCBI36
NG_031854.1:g.422939del
NG_031854.2:g.424863del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*633del MANE Select	ENSP00000477455.1:n.*633del
ENST00000636207.1:n.54+88del
ENST00000637214.1:c.69+46453del	ENSP00000489997.1:n.69+46453del
ENST00000609686.3:c.*633del	ENSP00000477455.1:n.*633del
NM_000834.3:c.*633del	NP_000825.2:n.*633del
XM_005253351.2:c.*633del	XP_005253408.1:n.*633del
XM_011520628.1:c.*633del	XP_011518930.1:n.*633del
XM_011520629.1:c.*633del	XP_011518931.1:n.*633del
XM_011520630.1:c.*633del	XP_011518932.1:n.*633del
NM_000834.4:c.*633del	NP_000825.2:n.*633del
XM_005253351.3:c.*633del	XP_005253408.1:n.*633del
XM_011520628.2:c.*633del	XP_011518930.1:n.*633del
XM_011520629.2:c.*633del	XP_011518931.1:n.*633del
XM_017019219.2:c.*633del	XP_016874708.1:n.*633del
NM_000834.5:c.*633del MANE Select	NP_000825.2:n.*633del