Canonical Allele Identifier: CA2317457799

Gene: GRIN3B

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1004902A= , CM000681.2:g.1004902A=	GRCh38
NC_000019.9:g.1004901A= , CM000681.1:g.1004901A=	GRCh37
NC_000019.8:g.955901A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000234389.3:c.1401A= MANE Select	ENSP00000234389.3:p.Ser467=
ENST00000588335.1:n.151A=
NM_138690.1:c.1401A=	NP_619635.1:p.Ser467=
NM_138690.2:c.1401A=	NP_619635.1:p.Ser467=
XM_017026243.2:c.-178A=	XP_016881732.1:n.-178A=
NM_138690.3:c.1401A= MANE Select	NP_619635.1:p.Ser467=