Canonical Allele Identifier: CA2592025413

Gene: GRIN2B

Linked Data

• gnomAD v3: 12-13562386-G-GCTACCTTTGTGCTCACATAGCCTCTTTTTGGTTCTCCCAGCTTCACTCAA
• gnomAD v4: 12-13562386-G-GCTACCTTTGTGCTCACATAGCCTCTTTTTGGTTCTCCCAGCTTCACTCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562387_13562436dup , CM000674.2:g.13562387_13562436dup	GRCh38
NC_000012.11:g.13715321_13715370dup , CM000674.1:g.13715321_13715370dup	GRCh37
NC_000012.10:g.13606588_13606637dup	NCBI36
NG_031854.1:g.422653_422702dup
NG_031854.2:g.424577_424626dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*347_*396dup MANE Select	ENSP00000477455.1:n.*347_*396dup
ENST00000637214.1:c.69+46167_69+46216dup	ENSP00000489997.1:n.69+46167_69+46216dup
ENST00000609686.3:c.*347_*396dup	ENSP00000477455.1:n.*347_*396dup
NM_000834.3:c.*347_*396dup	NP_000825.2:n.*347_*396dup
XM_005253351.2:c.*347_*396dup	XP_005253408.1:n.*347_*396dup
XM_011520628.1:c.*347_*396dup	XP_011518930.1:n.*347_*396dup
XM_011520629.1:c.*347_*396dup	XP_011518931.1:n.*347_*396dup
XM_011520630.1:c.*347_*396dup	XP_011518932.1:n.*347_*396dup
NM_000834.4:c.*347_*396dup	NP_000825.2:n.*347_*396dup
XM_005253351.3:c.*347_*396dup	XP_005253408.1:n.*347_*396dup
XM_011520628.2:c.*347_*396dup	XP_011518930.1:n.*347_*396dup
XM_011520629.2:c.*347_*396dup	XP_011518931.1:n.*347_*396dup
XM_017019219.2:c.*347_*396dup	XP_016874708.1:n.*347_*396dup
NM_000834.5:c.*347_*396dup MANE Select	NP_000825.2:n.*347_*396dup