Canonical Allele Identifier: CA915947907

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 763040
• ClinVar RCV Id: RCV001445785
• dbSNP Id: rs1591712751

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753924del , CM000674.2:g.13753924del	GRCh38
NC_000012.11:g.13906858del , CM000674.1:g.13906858del	GRCh37
NC_000012.10:g.13798125del	NCBI36
NG_031854.1:g.231169del
NG_031854.2:g.233093del

Transcript Alleles

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