Canonical Allele Identifier: CA384054050
Gene: GRIN2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13753690C>A , CM000674.2:g.13753690C>A GRCh38
NC_000012.11:g.13906624C>A , CM000674.1:g.13906624C>A GRCh37
NC_000012.10:g.13797891C>A NCBI36
NG_031854.1:g.231399G>T
NG_031854.2:g.233323G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.637G>T MANE Select ENSP00000477455.1:p.Asp213Tyr
ENST00000630791.2:c.637G>T ENSP00000486677.2:p.Asp213Tyr
ENST00000609686.3:c.637G>T ENSP00000477455.1:p.Asp213Tyr
NM_000834.3:c.637G>T NP_000825.2:p.Asp213Tyr
XM_011520628.1:c.637G>T XP_011518930.1:p.Asp213Tyr
XM_011520629.1:c.637G>T XP_011518931.1:p.Asp213Tyr
XM_011520630.1:c.637G>T XP_011518932.1:p.Asp213Tyr
NM_000834.4:c.637G>T NP_000825.2:p.Asp213Tyr
XM_011520628.2:c.637G>T XP_011518930.1:p.Asp213Tyr
XM_011520629.2:c.637G>T XP_011518931.1:p.Asp213Tyr
XM_017019219.2:c.637G>T XP_016874708.1:p.Asp213Tyr
NM_000834.5:c.637G>T MANE Select NP_000825.2:p.Asp213Tyr