Canonical Allele Identifier: CA2575085682

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13608904-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608907del , CM000674.2:g.13608907del	GRCh38
NC_000012.11:g.13761841del , CM000674.1:g.13761841del	GRCh37
NC_000012.10:g.13653108del	NCBI36
NG_031854.1:g.376184del
NG_031854.2:g.378108del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-73del MANE Select	ENSP00000477455.1:n.1781-73del
ENST00000628166.2:n.41-73del
ENST00000609686.3:c.1781-73del	ENSP00000477455.1:n.1781-73del
ENST00000628166.1:n.41-73del
NM_000834.3:c.1781-73del	NP_000825.2:n.1781-73del
XM_011520628.1:c.1781-73del	XP_011518930.1:n.1781-73del
XM_011520629.1:c.1781-73del	XP_011518931.1:n.1781-73del
XM_011520630.1:c.1781-73del	XP_011518932.1:n.1781-73del
XR_931372.1:n.179-6191del
XR_931373.1:n.318+150del
NM_000834.4:c.1781-73del	NP_000825.2:n.1781-73del
XM_011520628.2:c.1781-73del	XP_011518930.1:n.1781-73del
XM_011520629.2:c.1781-73del	XP_011518931.1:n.1781-73del
XM_017019219.2:c.1781-73del	XP_016874708.1:n.1781-73del
XR_001749013.1:n.457+150del
XR_931372.2:n.316-6191del
XR_931373.2:n.457+150del
NM_000834.5:c.1781-73del MANE Select	NP_000825.2:n.1781-73del