Canonical Allele Identifier: CA2317457800
Gene: GRIN3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1004903G= , CM000681.2:g.1004903G= GRCh38
NC_000019.9:g.1004902G= , CM000681.1:g.1004902G= GRCh37
NC_000019.8:g.955902G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234389.3:c.1402G= MANE Select ENSP00000234389.3:p.Ala468=
ENST00000588335.1:n.152G=
NM_138690.1:c.1402G= NP_619635.1:p.Ala468=
NM_138690.2:c.1402G= NP_619635.1:p.Ala468=
XM_017026243.2:c.-177G= XP_016881732.1:n.-177G=
NM_138690.3:c.1402G= MANE Select NP_619635.1:p.Ala468=