Canonical Allele Identifier: CA603495896

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1252502709
• gnomAD v2: 12-14018697-AC-A
• gnomAD v3: 12-13865763-AC-A
• gnomAD v4: 12-13865763-AC-A
• MyVariant Identifiers: chr12:g.14018698del (hg19) ; chr12:g.13865764del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13865766del , CM000674.2:g.13865766del	GRCh38
NC_000012.11:g.14018700del , CM000674.1:g.14018700del	GRCh37
NC_000012.10:g.13909967del	NCBI36
NG_031854.1:g.119325del
NG_031854.2:g.121249del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.411+34del MANE Select	ENSP00000477455.1:n.411+34del
ENST00000630791.2:c.411+34del	ENSP00000486677.2:n.411+34del
ENST00000609686.3:c.411+34del	ENSP00000477455.1:n.411+34del
NM_000834.3:c.411+34del	NP_000825.2:n.411+34del
XM_011520628.1:c.411+34del	XP_011518930.1:n.411+34del
XM_011520629.1:c.411+34del	XP_011518931.1:n.411+34del
XM_011520630.1:c.411+34del	XP_011518932.1:n.411+34del
NM_000834.4:c.411+34del	NP_000825.2:n.411+34del
XM_011520628.2:c.411+34del	XP_011518930.1:n.411+34del
XM_011520629.2:c.411+34del	XP_011518931.1:n.411+34del
XM_017019219.2:c.411+34del	XP_016874708.1:n.411+34del
NM_000834.5:c.411+34del MANE Select	NP_000825.2:n.411+34del