Canonical Allele Identifier: CA2617751466

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13615370-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615372_13615373del , CM000674.2:g.13615372_13615373del	GRCh38
NC_000012.11:g.13768306_13768307del , CM000674.1:g.13768306_13768307del	GRCh37
NC_000012.10:g.13659573_13659574del	NCBI36
NG_031854.1:g.369717_369718del
NG_031854.2:g.371641_371642del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1501-105_1501-104del MANE Select	ENSP00000477455.1:n.1501-105_1501-104del
ENST00000609686.3:c.1501-105_1501-104del	ENSP00000477455.1:n.1501-105_1501-104del
NM_000834.3:c.1501-105_1501-104del	NP_000825.2:n.1501-105_1501-104del
XM_011520628.1:c.1501-105_1501-104del	XP_011518930.1:n.1501-105_1501-104del
XM_011520629.1:c.1501-105_1501-104del	XP_011518931.1:n.1501-105_1501-104del
XM_011520630.1:c.1501-105_1501-104del	XP_011518932.1:n.1501-105_1501-104del
XR_931372.1:n.307+146_307+147del
XR_931373.1:n.447+146_447+147del
XR_931374.1:n.246+146_246+147del
NM_000834.4:c.1501-105_1501-104del	NP_000825.2:n.1501-105_1501-104del
XM_011520628.2:c.1501-105_1501-104del	XP_011518930.1:n.1501-105_1501-104del
XM_011520629.2:c.1501-105_1501-104del	XP_011518931.1:n.1501-105_1501-104del
XM_017019219.2:c.1501-105_1501-104del	XP_016874708.1:n.1501-105_1501-104del
XR_001749013.1:n.728+146_728+147del
XR_931372.2:n.444+146_444+147del
XR_931373.2:n.586+146_586+147del
NM_000834.5:c.1501-105_1501-104del MANE Select	NP_000825.2:n.1501-105_1501-104del