Canonical Allele Identifier: CA2017631051
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981740_13981742delinsCCG , CM000674.2:g.13981740_13981742delinsCCG GRCh38
NC_000012.11:g.14134674_14134676delinsCCG , CM000674.1:g.14134674_14134676delinsCCG GRCh37
NC_000012.10:g.14025941_14025943delinsCCG NCBI36
NG_031854.1:g.3347_3349delinsCGG
NG_031854.2:g.5271_5273delinsCGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000630791.2:c.-682-166_-682-164delinsCGG ENSP00000486677.2:n.-682-166_-682-164delinsCGG
ENST00000627535.2:c.-448+174_-448+176delinsCGG ENSP00000486411.1:n.-448+174_-448+176delinsCGG
ENST00000630791.1:c.-682-166_-682-164delinsCGG ENSP00000486677.1:n.-682-166_-682-164delinsCGG
XM_011520629.1:c.-682-166_-682-164delinsCGG XP_011518931.1:n.-682-166_-682-164delinsCGG
XM_011520628.2:c.-848_-846delinsCGG XP_011518930.1:n.-848_-846delinsCGG
XM_011520629.2:c.-682-166_-682-164delinsCGG XP_011518931.1:n.-682-166_-682-164delinsCGG