Canonical Allele Identifier: CA2317457804

Gene: GRIN3B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1004909C= , CM000681.2:g.1004909C=	GRCh38
NC_000019.9:g.1004908C= , CM000681.1:g.1004908C=	GRCh37
NC_000019.8:g.955908C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234389.3:c.1408C= MANE Select	ENSP00000234389.3:p.Arg470=
ENST00000588335.1:n.158C=
NM_138690.1:c.1408C=	NP_619635.1:p.Arg470=
NM_138690.2:c.1408C=	NP_619635.1:p.Arg470=
XM_017026243.2:c.-171C=	XP_016881732.1:n.-171C=
NM_138690.3:c.1408C= MANE Select	NP_619635.1:p.Arg470=