Canonical Allele Identifier: CA2588171773
Gene: GRIN3B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004894_1004915del , CM000681.2:g.1004894_1004915del GRCh38
NC_000019.9:g.1004893_1004914del , CM000681.1:g.1004893_1004914del GRCh37
NC_000019.8:g.955893_955914del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234389.3:c.1393_1414del MANE Select ENSP00000234389.3:p.Asn465CysfsTer?
ENST00000588335.1:n.143_164del
NM_138690.1:c.1393_1414del NP_619635.1:p.Asn465CysfsTer?
NM_138690.2:c.1393_1414del NP_619635.1:p.Asn465CysfsTer?
XM_017026243.2:c.-186_-165del XP_016881732.1:n.-186_-165del
NM_138690.3:c.1393_1414del MANE Select NP_619635.1:p.Asn465CysfsTer?