Canonical Allele Identifier: CA315046
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 205709
dbSNP Id: rs796052570

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13753879T>C , CM000674.2:g.13753879T>C GRCh38
NC_000012.11:g.13906813T>C , CM000674.1:g.13906813T>C GRCh37
NC_000012.10:g.13798080T>C NCBI36
NG_031854.1:g.231210A>G
NG_031854.2:g.233134A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.448A>G MANE Select ENSP00000477455.1:p.Ile150Val
ENST00000630791.2:c.448A>G ENSP00000486677.2:p.Ile150Val
ENST00000609686.3:c.448A>G ENSP00000477455.1:p.Ile150Val
NM_000834.3:c.448A>G NP_000825.2:p.Ile150Val
XM_011520628.1:c.448A>G XP_011518930.1:p.Ile150Val
XM_011520629.1:c.448A>G XP_011518931.1:p.Ile150Val
XM_011520630.1:c.448A>G XP_011518932.1:p.Ile150Val
NM_000834.4:c.448A>G NP_000825.2:p.Ile150Val
XM_011520628.2:c.448A>G XP_011518930.1:p.Ile150Val
XM_011520629.2:c.448A>G XP_011518931.1:p.Ile150Val
XM_017019219.2:c.448A>G XP_016874708.1:p.Ile150Val
NM_000834.5:c.448A>G MANE Select NP_000825.2:p.Ile150Val