Canonical Allele Identifier: CA383990497

Gene: GRIN2B

Linked Data

• MyVariant Identifiers: chr12:g.13716976G>T (hg19) ; chr12:g.13564042G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13564042G>T , CM000674.2:g.13564042G>T	GRCh38
NC_000012.11:g.13716976G>T , CM000674.1:g.13716976G>T	GRCh37
NC_000012.10:g.13608243G>T	NCBI36
NG_031854.1:g.421047C>A
NG_031854.2:g.422971C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.3196C>A MANE Select	ENSP00000477455.1:p.His1066Asn
ENST00000637214.1:c.69+44561C>A	ENSP00000489997.1:n.69+44561C>A
ENST00000609686.3:c.3196C>A	ENSP00000477455.1:p.His1066Asn
ENST00000628166.1:n.1456C>A
NM_000834.3:c.3196C>A	NP_000825.2:p.His1066Asn
XM_005253351.2:c.982C>A	XP_005253408.1:p.His328Asn
XM_011520628.1:c.3196C>A	XP_011518930.1:p.His1066Asn
XM_011520629.1:c.3196C>A	XP_011518931.1:p.His1066Asn
XM_011520630.1:c.3196C>A	XP_011518932.1:p.His1066Asn
NM_000834.4:c.3196C>A	NP_000825.2:p.His1066Asn
XM_005253351.3:c.982C>A	XP_005253408.1:p.His328Asn
XM_011520628.2:c.3196C>A	XP_011518930.1:p.His1066Asn
XM_011520629.2:c.3196C>A	XP_011518931.1:p.His1066Asn
XM_017019219.2:c.3196C>A	XP_016874708.1:p.His1066Asn
NM_000834.5:c.3196C>A MANE Select	NP_000825.2:p.His1066Asn