Canonical Allele Identifier: CA944929922
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1948556952

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13562432_13562435del , CM000674.2:g.13562432_13562435del GRCh38
NC_000012.11:g.13715366_13715369del , CM000674.1:g.13715366_13715369del GRCh37
NC_000012.10:g.13606633_13606636del NCBI36
NG_031854.1:g.422657_422660del
NG_031854.2:g.424581_424584del

Transcript Alleles

HGVS Amino-acid change
ENST00000609686.4:c.*351_*354del MANE Select ENSP00000477455.1:n.*351_*354del
ENST00000637214.1:c.69+46171_69+46174del ENSP00000489997.1:n.69+46171_69+46174del
ENST00000609686.3:c.*351_*354del ENSP00000477455.1:n.*351_*354del
NM_000834.3:c.*351_*354del NP_000825.2:n.*351_*354del
XM_005253351.2:c.*351_*354del XP_005253408.1:n.*351_*354del
XM_011520628.1:c.*351_*354del XP_011518930.1:n.*351_*354del
XM_011520629.1:c.*351_*354del XP_011518931.1:n.*351_*354del
XM_011520630.1:c.*351_*354del XP_011518932.1:n.*351_*354del
NM_000834.4:c.*351_*354del NP_000825.2:n.*351_*354del
XM_005253351.3:c.*351_*354del XP_005253408.1:n.*351_*354del
XM_011520628.2:c.*351_*354del XP_011518930.1:n.*351_*354del
XM_011520629.2:c.*351_*354del XP_011518931.1:n.*351_*354del
XM_017019219.2:c.*351_*354del XP_016874708.1:n.*351_*354del
NM_000834.5:c.*351_*354del MANE Select NP_000825.2:n.*351_*354del