Canonical Allele Identifier: CA384053029

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 2574918
• ClinVar RCV Id: RCV003319815
• MyVariant Identifiers: chr12:g.13906292G>T (hg19) ; chr12:g.13753358G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753358G>T , CM000674.2:g.13753358G>T	GRCh38
NC_000012.11:g.13906292G>T , CM000674.1:g.13906292G>T	GRCh37
NC_000012.10:g.13797559G>T	NCBI36
NG_031854.1:g.231731C>A
NG_031854.2:g.233655C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.969C>A MANE Select	ENSP00000477455.1:p.Asn323Lys
ENST00000630791.2:c.969C>A	ENSP00000486677.2:p.Asn323Lys
ENST00000609686.3:c.969C>A	ENSP00000477455.1:p.Asn323Lys
NM_000834.3:c.969C>A	NP_000825.2:p.Asn323Lys
XM_011520628.1:c.969C>A	XP_011518930.1:p.Asn323Lys
XM_011520629.1:c.969C>A	XP_011518931.1:p.Asn323Lys
XM_011520630.1:c.969C>A	XP_011518932.1:p.Asn323Lys
NM_000834.4:c.969C>A	NP_000825.2:p.Asn323Lys
XM_011520628.2:c.969C>A	XP_011518930.1:p.Asn323Lys
XM_011520629.2:c.969C>A	XP_011518931.1:p.Asn323Lys
XM_017019219.2:c.969C>A	XP_016874708.1:p.Asn323Lys
NM_000834.5:c.969C>A MANE Select	NP_000825.2:p.Asn323Lys