Canonical Allele Identifier: CA2017463009

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615260A= , CM000674.2:g.13615260A=	GRCh38
NC_000012.11:g.13768194A= , CM000674.1:g.13768194A=	GRCh37
NC_000012.10:g.13659461A=	NCBI36
NG_031854.1:g.369829T=
NG_031854.2:g.371753T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1508T= MANE Select	ENSP00000477455.1:p.Met503=
ENST00000609686.3:c.1508T=	ENSP00000477455.1:p.Met503=
NM_000834.3:c.1508T=	NP_000825.2:p.Met503=
XM_011520628.1:c.1508T=	XP_011518930.1:p.Met503=
XM_011520629.1:c.1508T=	XP_011518931.1:p.Met503=
XM_011520630.1:c.1508T=	XP_011518932.1:p.Met503=
XR_931372.1:n.307+34A=
XR_931373.1:n.447+34A=
XR_931374.1:n.246+34A=
NM_000834.4:c.1508T=	NP_000825.2:p.Met503=
XM_011520628.2:c.1508T=	XP_011518930.1:p.Met503=
XM_011520629.2:c.1508T=	XP_011518931.1:p.Met503=
XM_017019219.2:c.1508T=	XP_016874708.1:p.Met503=
XR_001749013.1:n.728+34A=
XR_931372.2:n.444+34A=
XR_931373.2:n.586+34A=
NM_000834.5:c.1508T= MANE Select	NP_000825.2:p.Met503=