Canonical Allele Identifier: CA2017437628
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13562329G= , CM000674.2:g.13562329G= GRCh38
NC_000012.11:g.13715263G= , CM000674.1:g.13715263G= GRCh37
NC_000012.10:g.13606530G= NCBI36
NG_031854.1:g.422760C=
NG_031854.2:g.424684C=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.*454C= MANE Select ENSP00000477455.1:n.*454C=
ENST00000637214.1:c.69+46274C= ENSP00000489997.1:n.69+46274C=
ENST00000609686.3:c.*454C= ENSP00000477455.1:n.*454C=
NM_000834.3:c.*454C= NP_000825.2:n.*454C=
XM_005253351.2:c.*454C= XP_005253408.1:n.*454C=
XM_011520628.1:c.*454C= XP_011518930.1:n.*454C=
XM_011520629.1:c.*454C= XP_011518931.1:n.*454C=
XM_011520630.1:c.*454C= XP_011518932.1:n.*454C=
NM_000834.4:c.*454C= NP_000825.2:n.*454C=
XM_005253351.3:c.*454C= XP_005253408.1:n.*454C=
XM_011520628.2:c.*454C= XP_011518930.1:n.*454C=
XM_011520629.2:c.*454C= XP_011518931.1:n.*454C=
XM_017019219.2:c.*454C= XP_016874708.1:n.*454C=
NM_000834.5:c.*454C= MANE Select NP_000825.2:n.*454C=