Canonical Allele Identifier: CA2017631032
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981714G= , CM000674.2:g.13981714G= GRCh38
NC_000012.11:g.14134648G= , CM000674.1:g.14134648G= GRCh37
NC_000012.10:g.14025915G= NCBI36
NG_031854.1:g.3375C=
NG_031854.2:g.5299C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000630791.2:c.-682-138C= ENSP00000486677.2:n.-682-138C=
ENST00000627535.2:c.-448+202C= ENSP00000486411.1:n.-448+202C=
ENST00000630791.1:c.-682-138C= ENSP00000486677.1:n.-682-138C=
XM_011520629.1:c.-682-138C= XP_011518931.1:n.-682-138C=
XM_011520628.2:c.-820C= XP_011518930.1:n.-820C=
XM_011520629.2:c.-682-138C= XP_011518931.1:n.-682-138C=