Canonical Allele Identifier: CA2017510037
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13719073C= , CM000674.2:g.13719073C= GRCh38
NC_000012.11:g.13872007C= , CM000674.1:g.13872007C= GRCh37
NC_000012.10:g.13763274C= NCBI36
NG_031854.1:g.266016G=
NG_031854.2:g.267940G=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1010+34244G= MANE Select ENSP00000477455.1:n.1010+34244G=
ENST00000630791.2:c.1010+34244G= ENSP00000486677.2:n.1010+34244G=
ENST00000609686.3:c.1010+34244G= ENSP00000477455.1:n.1010+34244G=
NM_000834.3:c.1010+34244G= NP_000825.2:n.1010+34244G=
XM_011520628.1:c.1010+34244G= XP_011518930.1:n.1010+34244G=
XM_011520629.1:c.1010+34244G= XP_011518931.1:n.1010+34244G=
XM_011520630.1:c.1010+34244G= XP_011518932.1:n.1010+34244G=
NM_000834.4:c.1010+34244G= NP_000825.2:n.1010+34244G=
XM_011520628.2:c.1010+34244G= XP_011518930.1:n.1010+34244G=
XM_011520629.2:c.1010+34244G= XP_011518931.1:n.1010+34244G=
XM_017019219.2:c.1010+34244G= XP_016874708.1:n.1010+34244G=
NM_000834.5:c.1010+34244G= MANE Select NP_000825.2:n.1010+34244G=