Canonical Allele Identifier: CA174970
Gene: GRIN2B HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 162087
ClinVar RCV Id: RCV000149505
dbSNP Id: rs672601378
COSMIC: COSM430810

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13615149C>T , CM000674.2:g.13615149C>T GRCh38
NC_000012.11:g.13768083C>T , CM000674.1:g.13768083C>T GRCh37
NC_000012.10:g.13659350C>T NCBI36
NG_031854.1:g.369940G>A
NG_031854.2:g.371864G>A

Transcript Alleles

HGVS Amino-acid change
NM_000834.3:c.1619G>A VV NP_000825.2:p.Arg540His
XM_011520628.1:c.1619G>A XP_011518930.1:p.Arg540His
XM_011520629.1:c.1619G>A XP_011518931.1:p.Arg540His
XM_011520630.1:c.1619G>A XP_011518932.1:p.Arg540His
XR_931372.1:n.230C>T
XR_931373.1:n.370C>T
XR_931374.1:n.169C>T
NM_000834.4:c.1619G>A VV NP_000825.2:p.Arg540His
XM_011520628.2:c.1619G>A XP_011518930.1:p.Arg540His
XM_011520629.2:c.1619G>A XP_011518931.1:p.Arg540His
XM_017019219.2:c.1619G>A XP_016874708.1:p.Arg540His
XR_001749013.1:n.651C>T
XR_931372.2:n.367C>T
XR_931373.2:n.509C>T
ENST00000609686.3:c.1619G>A ENSP00000477455.1:p.Arg540His