Canonical Allele Identifier: CA2017462834

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615110T= , CM000674.2:g.13615110T=	GRCh38
NC_000012.11:g.13768044T= , CM000674.1:g.13768044T=	GRCh37
NC_000012.10:g.13659311T=	NCBI36
NG_031854.1:g.369979A=
NG_031854.2:g.371903A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1654+4A= MANE Select	ENSP00000477455.1:n.1654+4A=
ENST00000609686.3:c.1654+4A=	ENSP00000477455.1:n.1654+4A=
NM_000834.3:c.1654+4A=	NP_000825.2:n.1654+4A=
XM_011520628.1:c.1654+4A=	XP_011518930.1:n.1654+4A=
XM_011520629.1:c.1654+4A=	XP_011518931.1:n.1654+4A=
XM_011520630.1:c.1654+4A=	XP_011518932.1:n.1654+4A=
XR_931372.1:n.191T=
XR_931373.1:n.331T=
XR_931374.1:n.130T=
NM_000834.4:c.1654+4A=	NP_000825.2:n.1654+4A=
XM_011520628.2:c.1654+4A=	XP_011518930.1:n.1654+4A=
XM_011520629.2:c.1654+4A=	XP_011518931.1:n.1654+4A=
XM_017019219.2:c.1654+4A=	XP_016874708.1:n.1654+4A=
XR_001749013.1:n.612T=
XR_931372.2:n.328T=
XR_931373.2:n.470T=
NM_000834.5:c.1654+4A= MANE Select	NP_000825.2:n.1654+4A=