Canonical Allele Identifier: CA2507535496

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608983_13608986dup , CM000674.2:g.13608983_13608986dup	GRCh38
NC_000012.11:g.13761917_13761920dup , CM000674.1:g.13761917_13761920dup	GRCh37
NC_000012.10:g.13653184_13653187dup	NCBI36
NG_031854.1:g.376105_376108dup
NG_031854.2:g.378029_378032dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-152_1781-149dup MANE Select	ENSP00000477455.1:n.1781-152_1781-149dup
ENST00000628166.2:n.41-152_41-149dup
ENST00000609686.3:c.1781-152_1781-149dup	ENSP00000477455.1:n.1781-152_1781-149dup
ENST00000628166.1:n.41-152_41-149dup
NM_000834.3:c.1781-152_1781-149dup	NP_000825.2:n.1781-152_1781-149dup
XM_011520628.1:c.1781-152_1781-149dup	XP_011518930.1:n.1781-152_1781-149dup
XM_011520629.1:c.1781-152_1781-149dup	XP_011518931.1:n.1781-152_1781-149dup
XM_011520630.1:c.1781-152_1781-149dup	XP_011518932.1:n.1781-152_1781-149dup
XR_931372.1:n.179-6115_179-6112dup
XR_931373.1:n.318+226_318+229dup
NM_000834.4:c.1781-152_1781-149dup	NP_000825.2:n.1781-152_1781-149dup
XM_011520628.2:c.1781-152_1781-149dup	XP_011518930.1:n.1781-152_1781-149dup
XM_011520629.2:c.1781-152_1781-149dup	XP_011518931.1:n.1781-152_1781-149dup
XM_017019219.2:c.1781-152_1781-149dup	XP_016874708.1:n.1781-152_1781-149dup
XR_001749013.1:n.457+226_457+229dup
XR_931372.2:n.316-6115_316-6112dup
XR_931373.2:n.457+226_457+229dup
NM_000834.5:c.1781-152_1781-149dup MANE Select	NP_000825.2:n.1781-152_1781-149dup