Canonical Allele Identifier: CA2017450743

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611800C= , CM000674.2:g.13611800C=	GRCh38
NC_000012.11:g.13764734C= , CM000674.1:g.13764734C=	GRCh37
NC_000012.10:g.13656001C=	NCBI36
NG_031854.1:g.373289G=
NG_031854.2:g.375213G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1705G= MANE Select	ENSP00000477455.1:p.Val569=
ENST00000609686.3:c.1705G=	ENSP00000477455.1:p.Val569=
NM_000834.3:c.1705G=	NP_000825.2:p.Val569=
XM_011520628.1:c.1705G=	XP_011518930.1:p.Val569=
XM_011520629.1:c.1705G=	XP_011518931.1:p.Val569=
XM_011520630.1:c.1705G=	XP_011518932.1:p.Val569=
XR_931372.1:n.179-3298C=
XR_931373.1:n.318+3043C=
XR_931374.1:n.117+1200C=
NM_000834.4:c.1705G=	NP_000825.2:p.Val569=
XM_011520628.2:c.1705G=	XP_011518930.1:p.Val569=
XM_011520629.2:c.1705G=	XP_011518931.1:p.Val569=
XM_017019219.2:c.1705G=	XP_016874708.1:p.Val569=
XR_001749013.1:n.599+1200C=
XR_931372.2:n.316-3298C=
XR_931373.2:n.457+3043C=
NM_000834.5:c.1705G= MANE Select	NP_000825.2:p.Val569=