Canonical Allele Identifier: CA2317457802

Gene: GRIN3B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1004905G= , CM000681.2:g.1004905G=	GRCh38
NC_000019.9:g.1004904G= , CM000681.1:g.1004904G=	GRCh37
NC_000019.8:g.955904G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234389.3:c.1404G= MANE Select	ENSP00000234389.3:p.Ala468=
ENST00000588335.1:n.154G=
NM_138690.1:c.1404G=	NP_619635.1:p.Ala468=
NM_138690.2:c.1404G=	NP_619635.1:p.Ala468=
XM_017026243.2:c.-175G=	XP_016881732.1:n.-175G=
NM_138690.3:c.1404G= MANE Select	NP_619635.1:p.Ala468=