Canonical Allele Identifier: CA13706288
Gene: GRIN2B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2268118

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13719110G>T , CM000674.2:g.13719110G>T GRCh38
NC_000012.11:g.13872044G>T , CM000674.1:g.13872044G>T GRCh37
NC_000012.10:g.13763311G>T NCBI36
NG_031854.1:g.265979C>A
NG_031854.2:g.267903C>A

Transcript Alleles

HGVS Amino-acid change
NM_000834.3:c.1010+34207C>A VV NP_000825.2:p.=
XM_011520628.1:c.1010+34207C>A XP_011518930.1:p.=
XM_011520629.1:c.1010+34207C>A XP_011518931.1:p.=
XM_011520630.1:c.1010+34207C>A XP_011518932.1:p.=
NM_000834.4:c.1010+34207C>A VV NP_000825.2:p.=
XM_011520628.2:c.1010+34207C>A XP_011518930.1:p.=
XM_011520629.2:c.1010+34207C>A XP_011518931.1:p.=
XM_017019219.2:c.1010+34207C>A XP_016874708.1:p.=
ENST00000609686.3:c.1010+34207C>A ENSP00000477455.1:p.=