Canonical Allele Identifier: CA2017631035
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981717C= , CM000674.2:g.13981717C= GRCh38
NC_000012.11:g.14134651C= , CM000674.1:g.14134651C= GRCh37
NC_000012.10:g.14025918C= NCBI36
NG_031854.1:g.3372G=
NG_031854.2:g.5296G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000630791.2:c.-682-141G= ENSP00000486677.2:n.-682-141G=
ENST00000627535.2:c.-448+199G= ENSP00000486411.1:n.-448+199G=
ENST00000630791.1:c.-682-141G= ENSP00000486677.1:n.-682-141G=
XM_011520629.1:c.-682-141G= XP_011518931.1:n.-682-141G=
XM_011520628.2:c.-823G= XP_011518930.1:n.-823G=
XM_011520629.2:c.-682-141G= XP_011518931.1:n.-682-141G=