Canonical Allele Identifier: CA2017631111
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981825C= , CM000674.2:g.13981825C= GRCh38
NC_000012.11:g.14134759C= , CM000674.1:g.14134759C= GRCh37
NC_000012.10:g.14026026C= NCBI36
NG_031854.1:g.3264G=
NG_031854.2:g.5188G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000630791.2:c.-683+91G= ENSP00000486677.2:n.-683+91G=
ENST00000627535.2:c.-448+91G= ENSP00000486411.1:n.-448+91G=
ENST00000630791.1:c.-683+91G= ENSP00000486677.1:n.-683+91G=
XM_011520629.1:c.-683+91G= XP_011518931.1:n.-683+91G=
XM_011520628.2:c.-931G= XP_011518930.1:n.-931G=
XM_011520629.2:c.-683+91G= XP_011518931.1:n.-683+91G=