Canonical Allele Identifier: CA2017437558

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1754224864

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562196_13562199del , CM000674.2:g.13562196_13562199del	GRCh38
NC_000012.11:g.13715130_13715133del , CM000674.1:g.13715130_13715133del	GRCh37
NC_000012.10:g.13606397_13606400del	NCBI36
NG_031854.1:g.422895_422898del
NG_031854.2:g.424819_424822del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*589_*592del MANE Select	ENSP00000477455.1:n.*589_*592del
ENST00000636207.1:n.54+44_54+47del
ENST00000637214.1:c.69+46409_69+46412del	ENSP00000489997.1:n.69+46409_69+46412del
ENST00000609686.3:c.*589_*592del	ENSP00000477455.1:n.*589_*592del
NM_000834.3:c.*589_*592del	NP_000825.2:n.*589_*592del
XM_005253351.2:c.*589_*592del	XP_005253408.1:n.*589_*592del
XM_011520628.1:c.*589_*592del	XP_011518930.1:n.*589_*592del
XM_011520629.1:c.*589_*592del	XP_011518931.1:n.*589_*592del
XM_011520630.1:c.*589_*592del	XP_011518932.1:n.*589_*592del
NM_000834.4:c.*589_*592del	NP_000825.2:n.*589_*592del
XM_005253351.3:c.*589_*592del	XP_005253408.1:n.*589_*592del
XM_011520628.2:c.*589_*592del	XP_011518930.1:n.*589_*592del
XM_011520629.2:c.*589_*592del	XP_011518931.1:n.*589_*592del
XM_017019219.2:c.*589_*592del	XP_016874708.1:n.*589_*592del
NM_000834.5:c.*589_*592del MANE Select	NP_000825.2:n.*589_*592del