Canonical Allele Identifier: CA2741231574
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13569929del , CM000674.2:g.13569929del GRCh38
NC_000012.11:g.13722863del , CM000674.1:g.13722863del GRCh37
NC_000012.10:g.13614130del NCBI36
NG_031854.1:g.415162del
NG_031854.2:g.417086del

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.2262del MANE Select ENSP00000477455.1:p.Lys755ArgfsTer?
ENST00000628166.2:n.522del
ENST00000637214.1:c.69+38676del ENSP00000489997.1:n.69+38676del
ENST00000609686.3:c.2262del ENSP00000477455.1:p.Lys755ArgfsTer?
ENST00000628166.1:n.522del
NM_000834.3:c.2262del NP_000825.2:p.Lys755ArgfsTer?
XM_005253351.2:c.48del XP_005253408.1:p.Lys17ArgfsTer?
XM_011520628.1:c.2262del XP_011518930.1:p.Lys755ArgfsTer?
XM_011520629.1:c.2262del XP_011518931.1:p.Lys755ArgfsTer?
XM_011520630.1:c.2262del XP_011518932.1:p.Lys755ArgfsTer?
NM_000834.4:c.2262del NP_000825.2:p.Lys755ArgfsTer?
XM_005253351.3:c.48del XP_005253408.1:p.Lys17ArgfsTer?
XM_011520628.2:c.2262del XP_011518930.1:p.Lys755ArgfsTer?
XM_011520629.2:c.2262del XP_011518931.1:p.Lys755ArgfsTer?
XM_017019219.2:c.2262del XP_016874708.1:p.Lys755ArgfsTer?
NM_000834.5:c.2262del MANE Select NP_000825.2:p.Lys755ArgfsTer?