Canonical Allele Identifier: CA2017418008
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13564220A= , CM000674.2:g.13564220A= GRCh38
NC_000012.11:g.13717154A= , CM000674.1:g.13717154A= GRCh37
NC_000012.10:g.13608421A= NCBI36
NG_031854.1:g.420869T=
NG_031854.2:g.422793T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.3018T= MANE Select ENSP00000477455.1:p.Cys1006=
ENST00000637214.1:c.69+44383T= ENSP00000489997.1:n.69+44383T=
ENST00000609686.3:c.3018T= ENSP00000477455.1:p.Cys1006=
ENST00000628166.1:n.1278T=
NM_000834.3:c.3018T= NP_000825.2:p.Cys1006=
XM_005253351.2:c.804T= XP_005253408.1:p.Cys268=
XM_011520628.1:c.3018T= XP_011518930.1:p.Cys1006=
XM_011520629.1:c.3018T= XP_011518931.1:p.Cys1006=
XM_011520630.1:c.3018T= XP_011518932.1:p.Cys1006=
NM_000834.4:c.3018T= NP_000825.2:p.Cys1006=
XM_005253351.3:c.804T= XP_005253408.1:p.Cys268=
XM_011520628.2:c.3018T= XP_011518930.1:p.Cys1006=
XM_011520629.2:c.3018T= XP_011518931.1:p.Cys1006=
XM_017019219.2:c.3018T= XP_016874708.1:p.Cys1006=
NM_000834.5:c.3018T= MANE Select NP_000825.2:p.Cys1006=