Canonical Allele Identifier: CA2017510036
Gene: GRIN2B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13719067G= , CM000674.2:g.13719067G= GRCh38
NC_000012.11:g.13872001G= , CM000674.1:g.13872001G= GRCh37
NC_000012.10:g.13763268G= NCBI36
NG_031854.1:g.266022C=
NG_031854.2:g.267946C=

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1010+34250C= MANE Select ENSP00000477455.1:n.1010+34250C=
ENST00000630791.2:c.1010+34250C= ENSP00000486677.2:n.1010+34250C=
ENST00000609686.3:c.1010+34250C= ENSP00000477455.1:n.1010+34250C=
NM_000834.3:c.1010+34250C= NP_000825.2:n.1010+34250C=
XM_011520628.1:c.1010+34250C= XP_011518930.1:n.1010+34250C=
XM_011520629.1:c.1010+34250C= XP_011518931.1:n.1010+34250C=
XM_011520630.1:c.1010+34250C= XP_011518932.1:n.1010+34250C=
NM_000834.4:c.1010+34250C= NP_000825.2:n.1010+34250C=
XM_011520628.2:c.1010+34250C= XP_011518930.1:n.1010+34250C=
XM_011520629.2:c.1010+34250C= XP_011518931.1:n.1010+34250C=
XM_017019219.2:c.1010+34250C= XP_016874708.1:n.1010+34250C=
NM_000834.5:c.1010+34250C= MANE Select NP_000825.2:n.1010+34250C=