Canonical Allele Identifier: CA315089
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 205731
ClinVar RCV Id: RCV001172372
dbSNP Id: rs1555110818

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13608706G>A , CM000674.2:g.13608706G>A GRCh38
NC_000012.11:g.13761640G>A , CM000674.1:g.13761640G>A GRCh37
NC_000012.10:g.13652907G>A NCBI36
NG_031854.1:g.376383C>T
NG_031854.2:g.378307C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.1907C>T MANE Select ENSP00000477455.1:p.Ala636Val
ENST00000628166.2:n.167C>T
ENST00000609686.3:c.1907C>T ENSP00000477455.1:p.Ala636Val
ENST00000628166.1:n.167C>T
NM_000834.3:c.1907C>T NP_000825.2:p.Ala636Val
XM_011520628.1:c.1907C>T XP_011518930.1:p.Ala636Val
XM_011520629.1:c.1907C>T XP_011518931.1:p.Ala636Val
XM_011520630.1:c.1907C>T XP_011518932.1:p.Ala636Val
XR_931372.1:n.179-6392G>A
XR_931373.1:n.267G>A
NM_000834.4:c.1907C>T NP_000825.2:p.Ala636Val
XM_011520628.2:c.1907C>T XP_011518930.1:p.Ala636Val
XM_011520629.2:c.1907C>T XP_011518931.1:p.Ala636Val
XM_017019219.2:c.1907C>T XP_016874708.1:p.Ala636Val
XR_001749013.1:n.406G>A
XR_931372.2:n.316-6392G>A
XR_931373.2:n.406G>A
NM_000834.5:c.1907C>T MANE Select NP_000825.2:p.Ala636Val