Canonical Allele Identifier: CA2017463393

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615549T= , CM000674.2:g.13615549T=	GRCh38
NC_000012.11:g.13768483T= , CM000674.1:g.13768483T=	GRCh37
NC_000012.10:g.13659750T=	NCBI36
NG_031854.1:g.369540A=
NG_031854.2:g.371464A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1444A= MANE Select	ENSP00000477455.1:p.Thr482=
ENST00000609686.3:c.1444A=	ENSP00000477455.1:p.Thr482=
NM_000834.3:c.1444A=	NP_000825.2:p.Thr482=
XM_011520628.1:c.1444A=	XP_011518930.1:p.Thr482=
XM_011520629.1:c.1444A=	XP_011518931.1:p.Thr482=
XM_011520630.1:c.1444A=	XP_011518932.1:p.Thr482=
XR_931372.1:n.307+323T=
XR_931373.1:n.447+323T=
XR_931374.1:n.246+323T=
NM_000834.4:c.1444A=	NP_000825.2:p.Thr482=
XM_011520628.2:c.1444A=	XP_011518930.1:p.Thr482=
XM_011520629.2:c.1444A=	XP_011518931.1:p.Thr482=
XM_017019219.2:c.1444A=	XP_016874708.1:p.Thr482=
XR_001749013.1:n.728+323T=
XR_931372.2:n.444+323T=
XR_931373.2:n.586+323T=
NM_000834.5:c.1444A= MANE Select	NP_000825.2:p.Thr482=