Canonical Allele Identifier: CA383992830

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 2933790
• ClinVar RCV Id: RCV003793348 ; RCV004366588
• dbSNP Id: rs926331767
• gnomAD v2: 12-13717266-G-A
• gnomAD v4: 12-13564332-G-A
• MyVariant Identifiers: chr12:g.13717266G>A (hg19) ; chr12:g.13564332G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13564332G>A , CM000674.2:g.13564332G>A	GRCh38
NC_000012.11:g.13717266G>A , CM000674.1:g.13717266G>A	GRCh37
NC_000012.10:g.13608533G>A	NCBI36
NG_031854.1:g.420757C>T
NG_031854.2:g.422681C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.2906C>T MANE Select	ENSP00000477455.1:p.Thr969Met
ENST00000637214.1:c.69+44271C>T	ENSP00000489997.1:n.69+44271C>T
ENST00000609686.3:c.2906C>T	ENSP00000477455.1:p.Thr969Met
ENST00000628166.1:n.1166C>T
NM_000834.3:c.2906C>T	NP_000825.2:p.Thr969Met
XM_005253351.2:c.692C>T	XP_005253408.1:p.Thr231Met
XM_011520628.1:c.2906C>T	XP_011518930.1:p.Thr969Met
XM_011520629.1:c.2906C>T	XP_011518931.1:p.Thr969Met
XM_011520630.1:c.2906C>T	XP_011518932.1:p.Thr969Met
NM_000834.4:c.2906C>T	NP_000825.2:p.Thr969Met
XM_005253351.3:c.692C>T	XP_005253408.1:p.Thr231Met
XM_011520628.2:c.2906C>T	XP_011518930.1:p.Thr969Met
XM_011520629.2:c.2906C>T	XP_011518931.1:p.Thr969Met
XM_017019219.2:c.2906C>T	XP_016874708.1:p.Thr969Met
NM_000834.5:c.2906C>T MANE Select	NP_000825.2:p.Thr969Met