Canonical Allele Identifier: CA2017414811
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13563125G= , CM000674.2:g.13563125G= GRCh38
NC_000012.11:g.13716059G= , CM000674.1:g.13716059G= GRCh37
NC_000012.10:g.13607326G= NCBI36
NG_031854.1:g.421964C=
NG_031854.2:g.423888C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.4113C= MANE Select ENSP00000477455.1:p.Tyr1371=
ENST00000637214.1:c.69+45478C= ENSP00000489997.1:n.69+45478C=
ENST00000609686.3:c.4113C= ENSP00000477455.1:p.Tyr1371=
ENST00000628166.1:n.2373C=
NM_000834.3:c.4113C= NP_000825.2:p.Tyr1371=
XM_005253351.2:c.1899C= XP_005253408.1:p.Tyr633=
XM_011520628.1:c.4113C= XP_011518930.1:p.Tyr1371=
XM_011520629.1:c.4113C= XP_011518931.1:p.Tyr1371=
XM_011520630.1:c.4113C= XP_011518932.1:p.Tyr1371=
NM_000834.4:c.4113C= NP_000825.2:p.Tyr1371=
XM_005253351.3:c.1899C= XP_005253408.1:p.Tyr633=
XM_011520628.2:c.4113C= XP_011518930.1:p.Tyr1371=
XM_011520629.2:c.4113C= XP_011518931.1:p.Tyr1371=
XM_017019219.2:c.4113C= XP_016874708.1:p.Tyr1371=
NM_000834.5:c.4113C= MANE Select NP_000825.2:p.Tyr1371=