Canonical Allele Identifier: CA2617753125

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13608976-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13608980_13608981del , CM000674.2:g.13608980_13608981del	GRCh38
NC_000012.11:g.13761914_13761915del , CM000674.1:g.13761914_13761915del	GRCh37
NC_000012.10:g.13653181_13653182del	NCBI36
NG_031854.1:g.376111_376112del
NG_031854.2:g.378035_378036del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1781-146_1781-145del MANE Select	ENSP00000477455.1:n.1781-146_1781-145del
ENST00000628166.2:n.41-146_41-145del
ENST00000609686.3:c.1781-146_1781-145del	ENSP00000477455.1:n.1781-146_1781-145del
ENST00000628166.1:n.41-146_41-145del
NM_000834.3:c.1781-146_1781-145del	NP_000825.2:n.1781-146_1781-145del
XM_011520628.1:c.1781-146_1781-145del	XP_011518930.1:n.1781-146_1781-145del
XM_011520629.1:c.1781-146_1781-145del	XP_011518931.1:n.1781-146_1781-145del
XM_011520630.1:c.1781-146_1781-145del	XP_011518932.1:n.1781-146_1781-145del
XR_931372.1:n.179-6118_179-6117del
XR_931373.1:n.318+223_318+224del
NM_000834.4:c.1781-146_1781-145del	NP_000825.2:n.1781-146_1781-145del
XM_011520628.2:c.1781-146_1781-145del	XP_011518930.1:n.1781-146_1781-145del
XM_011520629.2:c.1781-146_1781-145del	XP_011518931.1:n.1781-146_1781-145del
XM_017019219.2:c.1781-146_1781-145del	XP_016874708.1:n.1781-146_1781-145del
XR_001749013.1:n.457+223_457+224del
XR_931372.2:n.316-6118_316-6117del
XR_931373.2:n.457+223_457+224del
NM_000834.5:c.1781-146_1781-145del MANE Select	NP_000825.2:n.1781-146_1781-145del