Canonical Allele Identifier: CA2017450766
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13611829C= , CM000674.2:g.13611829C= GRCh38
NC_000012.11:g.13764763C= , CM000674.1:g.13764763C= GRCh37
NC_000012.10:g.13656030C= NCBI36
NG_031854.1:g.373260G=
NG_031854.2:g.375184G=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1676G= MANE Select ENSP00000477455.1:p.Trp559=
ENST00000609686.3:c.1676G= ENSP00000477455.1:p.Trp559=
NM_000834.3:c.1676G= NP_000825.2:p.Trp559=
XM_011520628.1:c.1676G= XP_011518930.1:p.Trp559=
XM_011520629.1:c.1676G= XP_011518931.1:p.Trp559=
XM_011520630.1:c.1676G= XP_011518932.1:p.Trp559=
XR_931372.1:n.179-3269C=
XR_931373.1:n.318+3072C=
XR_931374.1:n.117+1229C=
NM_000834.4:c.1676G= NP_000825.2:p.Trp559=
XM_011520628.2:c.1676G= XP_011518930.1:p.Trp559=
XM_011520629.2:c.1676G= XP_011518931.1:p.Trp559=
XM_017019219.2:c.1676G= XP_016874708.1:p.Trp559=
XR_001749013.1:n.599+1229C=
XR_931372.2:n.316-3269C=
XR_931373.2:n.457+3072C=
NM_000834.5:c.1676G= MANE Select NP_000825.2:p.Trp559=