Canonical Allele Identifier: CA15730150
Gene: GRIN2B HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1805502

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13561247A>G , CM000674.2:g.13561247A>G GRCh38
NC_000012.11:g.13714181A>G , CM000674.1:g.13714181A>G GRCh37
NC_000012.10:g.13605448A>G NCBI36
NG_031854.1:g.423842T>C
NG_031854.2:g.425766T>C

Transcript Alleles

HGVS Amino-acid change
XM_005253351.2:c.*1536T>C XP_005253408.1:p.=
XM_011520628.1:c.*1536T>C XP_011518930.1:p.=
XM_011520629.1:c.*1536T>C XP_011518931.1:p.=
XM_011520630.1:c.*1536T>C XP_011518932.1:p.=
NM_000834.4:c.*1536T>C VV NP_000825.2:p.=
XM_005253351.3:c.*1536T>C XP_005253408.1:p.=
XM_011520628.2:c.*1536T>C XP_011518930.1:p.=
XM_011520629.2:c.*1536T>C XP_011518931.1:p.=
XM_017019219.2:c.*1536T>C XP_016874708.1:p.=
ENST00000609686.3:c.*1536T>C ENSP00000477455.1:p.=