Canonical Allele Identifier: CA2017510018
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13719019A= , CM000674.2:g.13719019A= GRCh38
NC_000012.11:g.13871953A= , CM000674.1:g.13871953A= GRCh37
NC_000012.10:g.13763220A= NCBI36
NG_031854.1:g.266070T=
NG_031854.2:g.267994T=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1010+34298T= MANE Select ENSP00000477455.1:n.1010+34298T=
ENST00000630791.2:c.1010+34298T= ENSP00000486677.2:n.1010+34298T=
ENST00000609686.3:c.1010+34298T= ENSP00000477455.1:n.1010+34298T=
NM_000834.3:c.1010+34298T= NP_000825.2:n.1010+34298T=
XM_011520628.1:c.1010+34298T= XP_011518930.1:n.1010+34298T=
XM_011520629.1:c.1010+34298T= XP_011518931.1:n.1010+34298T=
XM_011520630.1:c.1010+34298T= XP_011518932.1:n.1010+34298T=
NM_000834.4:c.1010+34298T= NP_000825.2:n.1010+34298T=
XM_011520628.2:c.1010+34298T= XP_011518930.1:n.1010+34298T=
XM_011520629.2:c.1010+34298T= XP_011518931.1:n.1010+34298T=
XM_017019219.2:c.1010+34298T= XP_016874708.1:n.1010+34298T=
NM_000834.5:c.1010+34298T= MANE Select NP_000825.2:n.1010+34298T=