Canonical Allele Identifier: CA15725327
Gene: GRIN2B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs172677

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13944536A>G , CM000674.2:g.13944536A>G GRCh38
NC_000012.11:g.14097470A>G , CM000674.1:g.14097470A>G GRCh37
NC_000012.10:g.13988737A>G NCBI36
NG_031854.1:g.40553T>C
NG_031854.2:g.42477T>C

Transcript Alleles

HGVS Amino-acid change
NM_000834.3:c.-19+35392T>C VV NP_000825.2:p.=
XM_011520628.1:c.-19+35392T>C XP_011518930.1:p.=
XM_011520629.1:c.-19+35392T>C XP_011518931.1:p.=
XM_011520630.1:c.-19+35392T>C XP_011518932.1:p.=
NM_000834.4:c.-19+35392T>C VV
XM_011520628.2:c.-19+35392T>C
XM_011520629.2:c.-19+35392T>C
XM_017019219.2:c.-19+35392T>C XP_016874708.1:p.=
ENST00000609686.3:c.-19+35392T>C ENSP00000477455.1:p.=
ENST00000627535.2:c.-19+35392T>C ENSP00000486411.1:p.=
ENST00000630791.1:c.-19+35392T>C ENSP00000486677.1:p.=