Canonical Allele Identifier: CA315048
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 205710
dbSNP Id: rs796052571

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13608755C>T , CM000674.2:g.13608755C>T GRCh38
NC_000012.11:g.13761689C>T , CM000674.1:g.13761689C>T GRCh37
NC_000012.10:g.13652956C>T NCBI36
NG_031854.1:g.376334G>A
NG_031854.2:g.378258G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1858G>A MANE Select ENSP00000477455.1:p.Val620Met
ENST00000628166.2:n.118G>A
ENST00000609686.3:c.1858G>A ENSP00000477455.1:p.Val620Met
ENST00000628166.1:n.118G>A
NM_000834.3:c.1858G>A NP_000825.2:p.Val620Met
XM_011520628.1:c.1858G>A XP_011518930.1:p.Val620Met
XM_011520629.1:c.1858G>A XP_011518931.1:p.Val620Met
XM_011520630.1:c.1858G>A XP_011518932.1:p.Val620Met
XR_931372.1:n.179-6343C>T
XR_931373.1:n.316C>T
NM_000834.4:c.1858G>A NP_000825.2:p.Val620Met
XM_011520628.2:c.1858G>A XP_011518930.1:p.Val620Met
XM_011520629.2:c.1858G>A XP_011518931.1:p.Val620Met
XM_017019219.2:c.1858G>A XP_016874708.1:p.Val620Met
XR_001749013.1:n.455C>T
XR_931372.2:n.316-6343C>T
XR_931373.2:n.455C>T
NM_000834.5:c.1858G>A MANE Select NP_000825.2:p.Val620Met