Canonical Allele Identifier: CA2017437568

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1948554360

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562210_13562211insTAT , CM000674.2:g.13562210_13562211insTAT	GRCh38
NC_000012.11:g.13715144_13715145insTAT , CM000674.1:g.13715144_13715145insTAT	GRCh37
NC_000012.10:g.13606411_13606412insTAT	NCBI36
NG_031854.1:g.422879_422880insTAA
NG_031854.2:g.424803_424804insTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*573_*574insTAA MANE Select	ENSP00000477455.1:n.*573_*574insTAA
ENST00000636207.1:n.54+28_54+29insTAA
ENST00000637214.1:c.69+46393_69+46394insTAA	ENSP00000489997.1:n.69+46393_69+46394insTAA
ENST00000609686.3:c.*573_*574insTAA	ENSP00000477455.1:n.*573_*574insTAA
NM_000834.3:c.*573_*574insTAA	NP_000825.2:n.*573_*574insTAA
XM_005253351.2:c.*573_*574insTAA	XP_005253408.1:n.*573_*574insTAA
XM_011520628.1:c.*573_*574insTAA	XP_011518930.1:n.*573_*574insTAA
XM_011520629.1:c.*573_*574insTAA	XP_011518931.1:n.*573_*574insTAA
XM_011520630.1:c.*573_*574insTAA	XP_011518932.1:n.*573_*574insTAA
NM_000834.4:c.*573_*574insTAA	NP_000825.2:n.*573_*574insTAA
XM_005253351.3:c.*573_*574insTAA	XP_005253408.1:n.*573_*574insTAA
XM_011520628.2:c.*573_*574insTAA	XP_011518930.1:n.*573_*574insTAA
XM_011520629.2:c.*573_*574insTAA	XP_011518931.1:n.*573_*574insTAA
XM_017019219.2:c.*573_*574insTAA	XP_016874708.1:n.*573_*574insTAA
NM_000834.5:c.*573_*574insTAA MANE Select	NP_000825.2:n.*573_*574insTAA