Canonical Allele Identifier: CA2017437686

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1948557359

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562452_13562453insGAAGGAT , CM000674.2:g.13562452_13562453insGAAGGAT	GRCh38
NC_000012.11:g.13715386_13715387insGAAGGAT , CM000674.1:g.13715386_13715387insGAAGGAT	GRCh37
NC_000012.10:g.13606653_13606654insGAAGGAT	NCBI36
NG_031854.1:g.422636_422637insATCCTTC
NG_031854.2:g.424560_424561insATCCTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*330_*331insATCCTTC MANE Select	ENSP00000477455.1:n.*330_*331insATCCTTC
ENST00000637214.1:c.69+46150_69+46151insATCCTTC	ENSP00000489997.1:n.69+46150_69+46151insA...
ENST00000609686.3:c.*330_*331insATCCTTC	ENSP00000477455.1:n.*330_*331insATCCTTC
NM_000834.3:c.*330_*331insATCCTTC	NP_000825.2:n.*330_*331insATCCTTC
XM_005253351.2:c.*330_*331insATCCTTC	XP_005253408.1:n.*330_*331insATCCTTC
XM_011520628.1:c.*330_*331insATCCTTC	XP_011518930.1:n.*330_*331insATCCTTC
XM_011520629.1:c.*330_*331insATCCTTC	XP_011518931.1:n.*330_*331insATCCTTC
XM_011520630.1:c.*330_*331insATCCTTC	XP_011518932.1:n.*330_*331insATCCTTC
NM_000834.4:c.*330_*331insATCCTTC	NP_000825.2:n.*330_*331insATCCTTC
XM_005253351.3:c.*330_*331insATCCTTC	XP_005253408.1:n.*330_*331insATCCTTC
XM_011520628.2:c.*330_*331insATCCTTC	XP_011518930.1:n.*330_*331insATCCTTC
XM_011520629.2:c.*330_*331insATCCTTC	XP_011518931.1:n.*330_*331insATCCTTC
XM_017019219.2:c.*330_*331insATCCTTC	XP_016874708.1:n.*330_*331insATCCTTC
NM_000834.5:c.*330_*331insATCCTTC MANE Select	NP_000825.2:n.*330_*331insATCCTTC