Canonical Allele Identifier: CA2017441390
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13571844G= , CM000674.2:g.13571844G= GRCh38
NC_000012.11:g.13724778G= , CM000674.1:g.13724778G= GRCh37
NC_000012.10:g.13616045G= NCBI36
NG_031854.1:g.413245C=
NG_031854.2:g.415169C=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.2131C= MANE Select ENSP00000477455.1:p.Gln711=
ENST00000628166.2:n.391C=
ENST00000637214.1:c.69+36759C= ENSP00000489997.1:n.69+36759C=
ENST00000609686.3:c.2131C= ENSP00000477455.1:p.Gln711=
ENST00000628166.1:n.391C=
NM_000834.3:c.2131C= NP_000825.2:p.Gln711=
XM_005253351.2:c.-43-1827C= XP_005253408.1:n.-43-1827C=
XM_011520628.1:c.2131C= XP_011518930.1:p.Gln711=
XM_011520629.1:c.2131C= XP_011518931.1:p.Gln711=
XM_011520630.1:c.2131C= XP_011518932.1:p.Gln711=
NM_000834.4:c.2131C= NP_000825.2:p.Gln711=
XM_005253351.3:c.-43-1827C= XP_005253408.1:n.-43-1827C=
XM_011520628.2:c.2131C= XP_011518930.1:p.Gln711=
XM_011520629.2:c.2131C= XP_011518931.1:p.Gln711=
XM_017019219.2:c.2131C= XP_016874708.1:p.Gln711=
NM_000834.5:c.2131C= MANE Select NP_000825.2:p.Gln711=