Canonical Allele Identifier: CA2740092337

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 2943983
• ClinVar RCV Id: RCV003803541

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13569829_13569838dup , CM000674.2:g.13569829_13569838dup	GRCh38
NC_000012.11:g.13722763_13722772dup , CM000674.1:g.13722763_13722772dup	GRCh37
NC_000012.10:g.13614030_13614039dup	NCBI36
NG_031854.1:g.415252_415261dup
NG_031854.2:g.417176_417185dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.2352_2359+2dup
ENST00000628166.2:n.612_619+2dup
ENST00000637214.1:c.69+38766_69+38775dup	ENSP00000489997.1:n.69+38766_69+38775dup
ENST00000609686.3:c.2352_2359+2dup
ENST00000628166.1:n.612_619+2dup
NM_000834.3:c.2352_2359+2dup
XM_005253351.2:c.138_145+2dup
XM_011520628.1:c.2352_2359+2dup
XM_011520629.1:c.2352_2359+2dup
XM_011520630.1:c.2352_2359+2dup
NM_000834.4:c.2352_2359+2dup
XM_005253351.3:c.138_145+2dup
XM_011520628.2:c.2352_2359+2dup
XM_011520629.2:c.2352_2359+2dup
XM_017019219.2:c.2352_2359+2dup
NM_000834.5:c.2352_2359+2dup