Canonical Allele Identifier: CA2017631058
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981755A= , CM000674.2:g.13981755A= GRCh38
NC_000012.11:g.14134689A= , CM000674.1:g.14134689A= GRCh37
NC_000012.10:g.14025956A= NCBI36
NG_031854.1:g.3334T=
NG_031854.2:g.5258T=

Transcript Alleles

HGVS Amino-acid change
ENST00000630791.2:c.-683+161T= ENSP00000486677.2:n.-683+161T=
ENST00000627535.2:c.-448+161T= ENSP00000486411.1:n.-448+161T=
ENST00000630791.1:c.-683+161T= ENSP00000486677.1:n.-683+161T=
XM_011520629.1:c.-683+161T= XP_011518931.1:n.-683+161T=
XM_011520628.2:c.-861T= XP_011518930.1:n.-861T=
XM_011520629.2:c.-683+161T= XP_011518931.1:n.-683+161T=