Canonical Allele Identifier: CA919027726

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1591638973

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608996_13608997del , CM000674.2:g.13608996_13608997del	GRCh38
NC_000012.11:g.13761930_13761931del , CM000674.1:g.13761930_13761931del	GRCh37
NC_000012.10:g.13653197_13653198del	NCBI36
NG_031854.1:g.376094_376095del
NG_031854.2:g.378018_378019del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-163_1781-162del MANE Select	ENSP00000477455.1:n.1781-163_1781-162del
ENST00000628166.2:n.41-163_41-162del
ENST00000609686.3:c.1781-163_1781-162del	ENSP00000477455.1:n.1781-163_1781-162del
ENST00000628166.1:n.41-163_41-162del
NM_000834.3:c.1781-163_1781-162del	NP_000825.2:n.1781-163_1781-162del
XM_011520628.1:c.1781-163_1781-162del	XP_011518930.1:n.1781-163_1781-162del
XM_011520629.1:c.1781-163_1781-162del	XP_011518931.1:n.1781-163_1781-162del
XM_011520630.1:c.1781-163_1781-162del	XP_011518932.1:n.1781-163_1781-162del
XR_931372.1:n.179-6102_179-6101del
XR_931373.1:n.318+239_318+240del
NM_000834.4:c.1781-163_1781-162del	NP_000825.2:n.1781-163_1781-162del
XM_011520628.2:c.1781-163_1781-162del	XP_011518930.1:n.1781-163_1781-162del
XM_011520629.2:c.1781-163_1781-162del	XP_011518931.1:n.1781-163_1781-162del
XM_017019219.2:c.1781-163_1781-162del	XP_016874708.1:n.1781-163_1781-162del
XR_001749013.1:n.457+239_457+240del
XR_931372.2:n.316-6102_316-6101del
XR_931373.2:n.457+239_457+240del
NM_000834.5:c.1781-163_1781-162del MANE Select	NP_000825.2:n.1781-163_1781-162del