Canonical Allele Identifier: CA384051446
Gene: GRIN2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13611758C>T , CM000674.2:g.13611758C>T GRCh38
NC_000012.11:g.13764692C>T , CM000674.1:g.13764692C>T GRCh37
NC_000012.10:g.13655959C>T NCBI36
NG_031854.1:g.373331G>A
NG_031854.2:g.375255G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.1747G>A MANE Select ENSP00000477455.1:p.Val583Met
ENST00000609686.3:c.1747G>A ENSP00000477455.1:p.Val583Met
NM_000834.3:c.1747G>A NP_000825.2:p.Val583Met
XM_011520628.1:c.1747G>A XP_011518930.1:p.Val583Met
XM_011520629.1:c.1747G>A XP_011518931.1:p.Val583Met
XM_011520630.1:c.1747G>A XP_011518932.1:p.Val583Met
XR_931372.1:n.179-3340C>T
XR_931373.1:n.318+3001C>T
XR_931374.1:n.117+1158C>T
NM_000834.4:c.1747G>A NP_000825.2:p.Val583Met
XM_011520628.2:c.1747G>A XP_011518930.1:p.Val583Met
XM_011520629.2:c.1747G>A XP_011518931.1:p.Val583Met
XM_017019219.2:c.1747G>A XP_016874708.1:p.Val583Met
XR_001749013.1:n.599+1158C>T
XR_931372.2:n.316-3340C>T
XR_931373.2:n.457+3001C>T
NM_000834.5:c.1747G>A MANE Select NP_000825.2:p.Val583Met