Canonical Allele Identifier: CA2617757460

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13754038-T-TTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13754039_13754040insTAT , CM000674.2:g.13754039_13754040insTAT	GRCh38
NC_000012.11:g.13906973_13906974insTAT , CM000674.1:g.13906973_13906974insTAT	GRCh37
NC_000012.10:g.13798240_13798241insTAT	NCBI36
NG_031854.1:g.231050_231051insTAA
NG_031854.2:g.232974_232975insTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.412-124_412-123insTAA MANE Select	ENSP00000477455.1:n.412-124_412-123insTAA
ENST00000630791.2:c.412-124_412-123insTAA	ENSP00000486677.2:n.412-124_412-123insTAA
ENST00000609686.3:c.412-124_412-123insTAA	ENSP00000477455.1:n.412-124_412-123insTAA
NM_000834.3:c.412-124_412-123insTAA	NP_000825.2:n.412-124_412-123insTAA
XM_011520628.1:c.412-124_412-123insTAA	XP_011518930.1:n.412-124_412-123insTAA
XM_011520629.1:c.412-124_412-123insTAA	XP_011518931.1:n.412-124_412-123insTAA
XM_011520630.1:c.412-124_412-123insTAA	XP_011518932.1:n.412-124_412-123insTAA
NM_000834.4:c.412-124_412-123insTAA	NP_000825.2:n.412-124_412-123insTAA
XM_011520628.2:c.412-124_412-123insTAA	XP_011518930.1:n.412-124_412-123insTAA
XM_011520629.2:c.412-124_412-123insTAA	XP_011518931.1:n.412-124_412-123insTAA
XM_017019219.2:c.412-124_412-123insTAA	XP_016874708.1:n.412-124_412-123insTAA
NM_000834.5:c.412-124_412-123insTAA MANE Select	NP_000825.2:n.412-124_412-123insTAA