Canonical Allele Identifier: CA130435
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 39658
ClinVar RCV Id: RCV000032862
dbSNP Id: rs397514555

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13615626C>T , CM000674.2:g.13615626C>T GRCh38
NC_000012.11:g.13768560C>T , CM000674.1:g.13768560C>T GRCh37
NC_000012.10:g.13659827C>T NCBI36
NG_031854.1:g.369463G>A
NG_031854.2:g.371387G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.1367G>A MANE Select ENSP00000477455.1:p.Cys456Tyr
ENST00000630791.2:c.1367G>A ENSP00000486677.2:p.Cys456Tyr
ENST00000609686.3:c.1367G>A ENSP00000477455.1:p.Cys456Tyr
NM_000834.3:c.1367G>A NP_000825.2:p.Cys456Tyr
XM_011520628.1:c.1367G>A XP_011518930.1:p.Cys456Tyr
XM_011520629.1:c.1367G>A XP_011518931.1:p.Cys456Tyr
XM_011520630.1:c.1367G>A XP_011518932.1:p.Cys456Tyr
XR_931372.1:n.307+400C>T
XR_931373.1:n.447+400C>T
XR_931374.1:n.246+400C>T
NM_000834.4:c.1367G>A NP_000825.2:p.Cys456Tyr
XM_011520628.2:c.1367G>A XP_011518930.1:p.Cys456Tyr
XM_011520629.2:c.1367G>A XP_011518931.1:p.Cys456Tyr
XM_017019219.2:c.1367G>A XP_016874708.1:p.Cys456Tyr
XR_001749013.1:n.728+400C>T
XR_931372.2:n.444+400C>T
XR_931373.2:n.586+400C>T
NM_000834.5:c.1367G>A MANE Select NP_000825.2:p.Cys456Tyr