Canonical Allele Identifier: CA2017447883

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608774C= , CM000674.2:g.13608774C=	GRCh38
NC_000012.11:g.13761708C= , CM000674.1:g.13761708C=	GRCh37
NC_000012.10:g.13652975C=	NCBI36
NG_031854.1:g.376315G=
NG_031854.2:g.378239G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1839G= MANE Select	ENSP00000477455.1:p.Val613=
ENST00000628166.2:n.99G=
ENST00000609686.3:c.1839G=	ENSP00000477455.1:p.Val613=
ENST00000628166.1:n.99G=
NM_000834.3:c.1839G=	NP_000825.2:p.Val613=
XM_011520628.1:c.1839G=	XP_011518930.1:p.Val613=
XM_011520629.1:c.1839G=	XP_011518931.1:p.Val613=
XM_011520630.1:c.1839G=	XP_011518932.1:p.Val613=
XR_931372.1:n.179-6324C=
XR_931373.1:n.318+17C=
NM_000834.4:c.1839G=	NP_000825.2:p.Val613=
XM_011520628.2:c.1839G=	XP_011518930.1:p.Val613=
XM_011520629.2:c.1839G=	XP_011518931.1:p.Val613=
XM_017019219.2:c.1839G=	XP_016874708.1:p.Val613=
XR_001749013.1:n.457+17C=
XR_931372.2:n.316-6324C=
XR_931373.2:n.457+17C=
NM_000834.5:c.1839G= MANE Select	NP_000825.2:p.Val613=