Canonical Allele Identifier: CA2617751428

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13615351-T-TTCTTTGTATA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615352_13615361dup , CM000674.2:g.13615352_13615361dup	GRCh38
NC_000012.11:g.13768286_13768295dup , CM000674.1:g.13768286_13768295dup	GRCh37
NC_000012.10:g.13659553_13659562dup	NCBI36
NG_031854.1:g.369728_369737dup
NG_031854.2:g.371652_371661dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1501-94_1501-85dup MANE Select	ENSP00000477455.1:n.1501-94_1501-85dup
ENST00000609686.3:c.1501-94_1501-85dup	ENSP00000477455.1:n.1501-94_1501-85dup
NM_000834.3:c.1501-94_1501-85dup	NP_000825.2:n.1501-94_1501-85dup
XM_011520628.1:c.1501-94_1501-85dup	XP_011518930.1:n.1501-94_1501-85dup
XM_011520629.1:c.1501-94_1501-85dup	XP_011518931.1:n.1501-94_1501-85dup
XM_011520630.1:c.1501-94_1501-85dup	XP_011518932.1:n.1501-94_1501-85dup
XR_931372.1:n.307+126_307+135dup
XR_931373.1:n.447+126_447+135dup
XR_931374.1:n.246+126_246+135dup
NM_000834.4:c.1501-94_1501-85dup	NP_000825.2:n.1501-94_1501-85dup
XM_011520628.2:c.1501-94_1501-85dup	XP_011518930.1:n.1501-94_1501-85dup
XM_011520629.2:c.1501-94_1501-85dup	XP_011518931.1:n.1501-94_1501-85dup
XM_017019219.2:c.1501-94_1501-85dup	XP_016874708.1:n.1501-94_1501-85dup
XR_001749013.1:n.728+126_728+135dup
XR_931372.2:n.444+126_444+135dup
XR_931373.2:n.586+126_586+135dup
NM_000834.5:c.1501-94_1501-85dup MANE Select	NP_000825.2:n.1501-94_1501-85dup