Canonical Allele Identifier: CA1139662531

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 951364
• ClinVar RCV Id: RCV001223256
• dbSNP Id: rs201154780

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615672A>T , CM000674.2:g.13615672A>T	GRCh38
NC_000012.11:g.13768606A>T , CM000674.1:g.13768606A>T	GRCh37
NC_000012.10:g.13659873A>T	NCBI36
NG_031854.1:g.369417T>A
NG_031854.2:g.371341T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1329-8T>A MANE Select	ENSP00000477455.1:n.1329-8T>A
ENST00000630791.2:c.1329-8T>A	ENSP00000486677.2:n.1329-8T>A
ENST00000609686.3:c.1329-8T>A	ENSP00000477455.1:n.1329-8T>A
NM_000834.3:c.1329-8T>A	NP_000825.2:n.1329-8T>A
XM_011520628.1:c.1329-8T>A	XP_011518930.1:n.1329-8T>A
XM_011520629.1:c.1329-8T>A	XP_011518931.1:n.1329-8T>A
XM_011520630.1:c.1329-8T>A	XP_011518932.1:n.1329-8T>A
XR_931372.1:n.307+446A>T
XR_931373.1:n.447+446A>T
XR_931374.1:n.246+446A>T
NM_000834.4:c.1329-8T>A	NP_000825.2:n.1329-8T>A
XM_011520628.2:c.1329-8T>A	XP_011518930.1:n.1329-8T>A
XM_011520629.2:c.1329-8T>A	XP_011518931.1:n.1329-8T>A
XM_017019219.2:c.1329-8T>A	XP_016874708.1:n.1329-8T>A
XR_001749013.1:n.728+446A>T
XR_931372.2:n.444+446A>T
XR_931373.2:n.586+446A>T
NM_000834.5:c.1329-8T>A MANE Select	NP_000825.2:n.1329-8T>A