Canonical Allele Identifier: CA2017418673
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13564478G= , CM000674.2:g.13564478G= GRCh38
NC_000012.11:g.13717412G= , CM000674.1:g.13717412G= GRCh37
NC_000012.10:g.13608679G= NCBI36
NG_031854.1:g.420611C=
NG_031854.2:g.422535C=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.2760C= MANE Select ENSP00000477455.1:p.Ser920=
ENST00000637214.1:c.69+44125C= ENSP00000489997.1:n.69+44125C=
ENST00000609686.3:c.2760C= ENSP00000477455.1:p.Ser920=
ENST00000628166.1:n.1020C=
NM_000834.3:c.2760C= NP_000825.2:p.Ser920=
XM_005253351.2:c.546C= XP_005253408.1:p.Ser182=
XM_011520628.1:c.2760C= XP_011518930.1:p.Ser920=
XM_011520629.1:c.2760C= XP_011518931.1:p.Ser920=
XM_011520630.1:c.2760C= XP_011518932.1:p.Ser920=
NM_000834.4:c.2760C= NP_000825.2:p.Ser920=
XM_005253351.3:c.546C= XP_005253408.1:p.Ser182=
XM_011520628.2:c.2760C= XP_011518930.1:p.Ser920=
XM_011520629.2:c.2760C= XP_011518931.1:p.Ser920=
XM_017019219.2:c.2760C= XP_016874708.1:p.Ser920=
NM_000834.5:c.2760C= MANE Select NP_000825.2:p.Ser920=