Canonical Allele Identifier: CA233011654
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1805539

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13617256G>T , CM000674.2:g.13617256G>T GRCh38
NC_000012.11:g.13770190G>T , CM000674.1:g.13770190G>T GRCh37
NC_000012.10:g.13661457G>T NCBI36
NG_031854.1:g.367833C>A
NG_031854.2:g.369757C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1126-599C>A MANE Select ENSP00000477455.1:n.1126-599C>A
ENST00000630791.2:c.1126-599C>A ENSP00000486677.2:n.1126-599C>A
ENST00000609686.3:c.1126-599C>A ENSP00000477455.1:n.1126-599C>A
NM_000834.3:c.1126-599C>A NP_000825.2:n.1126-599C>A
XM_011520628.1:c.1126-599C>A XP_011518930.1:n.1126-599C>A
XM_011520629.1:c.1126-599C>A XP_011518931.1:n.1126-599C>A
XM_011520630.1:c.1126-599C>A XP_011518932.1:n.1126-599C>A
XR_931372.1:n.307+2030G>T
XR_931373.1:n.447+2030G>T
XR_931374.1:n.246+2030G>T
NM_000834.4:c.1126-599C>A NP_000825.2:n.1126-599C>A
XM_011520628.2:c.1126-599C>A XP_011518930.1:n.1126-599C>A
XM_011520629.2:c.1126-599C>A XP_011518931.1:n.1126-599C>A
XM_017019219.2:c.1126-599C>A XP_016874708.1:n.1126-599C>A
XR_001749013.1:n.728+2030G>T
XR_931372.2:n.444+2030G>T
XR_931373.2:n.586+2030G>T
NM_000834.5:c.1126-599C>A MANE Select NP_000825.2:n.1126-599C>A