Canonical Allele Identifier: CA2794615800

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13614904C>T , CM000674.2:g.13614904C>T	GRCh38
NC_000012.11:g.13767838C>T , CM000674.1:g.13767838C>T	GRCh37
NC_000012.10:g.13659105C>T	NCBI36
NG_031854.1:g.370185G>A
NG_031854.2:g.372109G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1654+210G>A MANE Select	ENSP00000477455.1:n.1654+210G>A
ENST00000609686.3:c.1654+210G>A	ENSP00000477455.1:n.1654+210G>A
NM_000834.3:c.1654+210G>A	NP_000825.2:n.1654+210G>A
XM_011520628.1:c.1654+210G>A	XP_011518930.1:n.1654+210G>A
XM_011520629.1:c.1654+210G>A	XP_011518931.1:n.1654+210G>A
XM_011520630.1:c.1654+210G>A	XP_011518932.1:n.1654+210G>A
XR_931372.1:n.179-194C>T
XR_931373.1:n.319-194C>T
XR_931374.1:n.118-194C>T
NM_000834.4:c.1654+210G>A	NP_000825.2:n.1654+210G>A
XM_011520628.2:c.1654+210G>A	XP_011518930.1:n.1654+210G>A
XM_011520629.2:c.1654+210G>A	XP_011518931.1:n.1654+210G>A
XM_017019219.2:c.1654+210G>A	XP_016874708.1:n.1654+210G>A
XR_001749013.1:n.600-194C>T
XR_931372.2:n.316-194C>T
XR_931373.2:n.458-194C>T
NM_000834.5:c.1654+210G>A MANE Select	NP_000825.2:n.1654+210G>A