Canonical Allele Identifier: CA2617753133

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13608980-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608985_13608986del , CM000674.2:g.13608985_13608986del	GRCh38
NC_000012.11:g.13761919_13761920del , CM000674.1:g.13761919_13761920del	GRCh37
NC_000012.10:g.13653186_13653187del	NCBI36
NG_031854.1:g.376107_376108del
NG_031854.2:g.378031_378032del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-150_1781-149del MANE Select	ENSP00000477455.1:n.1781-150_1781-149del
ENST00000628166.2:n.41-150_41-149del
ENST00000609686.3:c.1781-150_1781-149del	ENSP00000477455.1:n.1781-150_1781-149del
ENST00000628166.1:n.41-150_41-149del
NM_000834.3:c.1781-150_1781-149del	NP_000825.2:n.1781-150_1781-149del
XM_011520628.1:c.1781-150_1781-149del	XP_011518930.1:n.1781-150_1781-149del
XM_011520629.1:c.1781-150_1781-149del	XP_011518931.1:n.1781-150_1781-149del
XM_011520630.1:c.1781-150_1781-149del	XP_011518932.1:n.1781-150_1781-149del
XR_931372.1:n.179-6113_179-6112del
XR_931373.1:n.318+228_318+229del
NM_000834.4:c.1781-150_1781-149del	NP_000825.2:n.1781-150_1781-149del
XM_011520628.2:c.1781-150_1781-149del	XP_011518930.1:n.1781-150_1781-149del
XM_011520629.2:c.1781-150_1781-149del	XP_011518931.1:n.1781-150_1781-149del
XM_017019219.2:c.1781-150_1781-149del	XP_016874708.1:n.1781-150_1781-149del
XR_001749013.1:n.457+228_457+229del
XR_931372.2:n.316-6113_316-6112del
XR_931373.2:n.457+228_457+229del
NM_000834.5:c.1781-150_1781-149del MANE Select	NP_000825.2:n.1781-150_1781-149del