Canonical Allele Identifier: CA383992172

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1555102403
• MyVariant Identifiers: chr12:g.13717081T>A (hg19) ; chr12:g.13564147T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13564147T>A , CM000674.2:g.13564147T>A	GRCh38
NC_000012.11:g.13717081T>A , CM000674.1:g.13717081T>A	GRCh37
NC_000012.10:g.13608348T>A	NCBI36
NG_031854.1:g.420942A>T
NG_031854.2:g.422866A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.3091A>T MANE Select	ENSP00000477455.1:p.Lys1031Ter
ENST00000637214.1:c.69+44456A>T	ENSP00000489997.1:n.69+44456A>T
ENST00000609686.3:c.3091A>T	ENSP00000477455.1:p.Lys1031Ter
ENST00000628166.1:n.1351A>T
NM_000834.3:c.3091A>T	NP_000825.2:p.Lys1031Ter
XM_005253351.2:c.877A>T	XP_005253408.1:p.Lys293Ter
XM_011520628.1:c.3091A>T	XP_011518930.1:p.Lys1031Ter
XM_011520629.1:c.3091A>T	XP_011518931.1:p.Lys1031Ter
XM_011520630.1:c.3091A>T	XP_011518932.1:p.Lys1031Ter
NM_000834.4:c.3091A>T	NP_000825.2:p.Lys1031Ter
XM_005253351.3:c.877A>T	XP_005253408.1:p.Lys293Ter
XM_011520628.2:c.3091A>T	XP_011518930.1:p.Lys1031Ter
XM_011520629.2:c.3091A>T	XP_011518931.1:p.Lys1031Ter
XM_017019219.2:c.3091A>T	XP_016874708.1:p.Lys1031Ter
NM_000834.5:c.3091A>T MANE Select	NP_000825.2:p.Lys1031Ter