Canonical Allele Identifier: CA384053692
Gene: GRIN2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13753597C>T , CM000674.2:g.13753597C>T GRCh38
NC_000012.11:g.13906531C>T , CM000674.1:g.13906531C>T GRCh37
NC_000012.10:g.13797798C>T NCBI36
NG_031854.1:g.231492G>A
NG_031854.2:g.233416G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.730G>A MANE Select ENSP00000477455.1:p.Ala244Thr
ENST00000630791.2:c.730G>A ENSP00000486677.2:p.Ala244Thr
ENST00000609686.3:c.730G>A ENSP00000477455.1:p.Ala244Thr
NM_000834.3:c.730G>A NP_000825.2:p.Ala244Thr
XM_011520628.1:c.730G>A XP_011518930.1:p.Ala244Thr
XM_011520629.1:c.730G>A XP_011518931.1:p.Ala244Thr
XM_011520630.1:c.730G>A XP_011518932.1:p.Ala244Thr
NM_000834.4:c.730G>A NP_000825.2:p.Ala244Thr
XM_011520628.2:c.730G>A XP_011518930.1:p.Ala244Thr
XM_011520629.2:c.730G>A XP_011518931.1:p.Ala244Thr
XM_017019219.2:c.730G>A XP_016874708.1:p.Ala244Thr
NM_000834.5:c.730G>A MANE Select NP_000825.2:p.Ala244Thr