Canonical Allele Identifier: CA384053587
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1863526741

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13753569C>A , CM000674.2:g.13753569C>A GRCh38
NC_000012.11:g.13906503C>A , CM000674.1:g.13906503C>A GRCh37
NC_000012.10:g.13797770C>A NCBI36
NG_031854.1:g.231520G>T
NG_031854.2:g.233444G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.758G>T MANE Select ENSP00000477455.1:p.Gly253Val
ENST00000630791.2:c.758G>T ENSP00000486677.2:p.Gly253Val
ENST00000609686.3:c.758G>T ENSP00000477455.1:p.Gly253Val
NM_000834.3:c.758G>T NP_000825.2:p.Gly253Val
XM_011520628.1:c.758G>T XP_011518930.1:p.Gly253Val
XM_011520629.1:c.758G>T XP_011518931.1:p.Gly253Val
XM_011520630.1:c.758G>T XP_011518932.1:p.Gly253Val
NM_000834.4:c.758G>T NP_000825.2:p.Gly253Val
XM_011520628.2:c.758G>T XP_011518930.1:p.Gly253Val
XM_011520629.2:c.758G>T XP_011518931.1:p.Gly253Val
XM_017019219.2:c.758G>T XP_016874708.1:p.Gly253Val
NM_000834.5:c.758G>T MANE Select NP_000825.2:p.Gly253Val