Canonical Allele Identifier: CA2317457801
Gene: GRIN3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004904C= , CM000681.2:g.1004904C= GRCh38
NC_000019.9:g.1004903C= , CM000681.1:g.1004903C= GRCh37
NC_000019.8:g.955903C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234389.3:c.1403C= MANE Select ENSP00000234389.3:p.Ala468=
ENST00000588335.1:n.153C=
NM_138690.1:c.1403C= NP_619635.1:p.Ala468=
NM_138690.2:c.1403C= NP_619635.1:p.Ala468=
XM_017026243.2:c.-176C= XP_016881732.1:n.-176C=
NM_138690.3:c.1403C= MANE Select NP_619635.1:p.Ala468=