Canonical Allele Identifier: CA2017436991
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13561171C= , CM000674.2:g.13561171C= GRCh38
NC_000012.11:g.13714105C= , CM000674.1:g.13714105C= GRCh37
NC_000012.10:g.13605372C= NCBI36
NG_031854.1:g.423918G=
NG_031854.2:g.425842G=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.*1612G= MANE Select ENSP00000477455.1:n.*1612G=
ENST00000637214.1:c.69+47432G= ENSP00000489997.1:n.69+47432G=
ENST00000609686.3:c.*1612G= ENSP00000477455.1:n.*1612G=
XM_005253351.2:c.*1612G= XP_005253408.1:n.*1612G=
XM_011520628.1:c.*1612G= XP_011518930.1:n.*1612G=
XM_011520629.1:c.*1612G= XP_011518931.1:n.*1612G=
XM_011520630.1:c.*1612G= XP_011518932.1:n.*1612G=
NM_000834.4:c.*1612G= NP_000825.2:n.*1612G=
XM_005253351.3:c.*1612G= XP_005253408.1:n.*1612G=
XM_011520628.2:c.*1612G= XP_011518930.1:n.*1612G=
XM_011520629.2:c.*1612G= XP_011518931.1:n.*1612G=
XM_017019219.2:c.*1612G= XP_016874708.1:n.*1612G=
NM_000834.5:c.*1612G= MANE Select NP_000825.2:n.*1612G=