Canonical Allele Identifier: CA2581062515

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562216T>C , CM000674.2:g.13562216T>C	GRCh38
NC_000012.11:g.13715150T>C , CM000674.1:g.13715150T>C	GRCh37
NC_000012.10:g.13606417T>C	NCBI36
NG_031854.1:g.422873A>G
NG_031854.2:g.424797A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*567A>G MANE Select	ENSP00000477455.1:n.*567A>G
ENST00000636207.1:n.54+22A>G
ENST00000637214.1:c.69+46387A>G	ENSP00000489997.1:n.69+46387A>G
ENST00000609686.3:c.*567A>G	ENSP00000477455.1:n.*567A>G
NM_000834.3:c.*567A>G	NP_000825.2:n.*567A>G
XM_005253351.2:c.*567A>G	XP_005253408.1:n.*567A>G
XM_011520628.1:c.*567A>G	XP_011518930.1:n.*567A>G
XM_011520629.1:c.*567A>G	XP_011518931.1:n.*567A>G
XM_011520630.1:c.*567A>G	XP_011518932.1:n.*567A>G
NM_000834.4:c.*567A>G	NP_000825.2:n.*567A>G
XM_005253351.3:c.*567A>G	XP_005253408.1:n.*567A>G
XM_011520628.2:c.*567A>G	XP_011518930.1:n.*567A>G
XM_011520629.2:c.*567A>G	XP_011518931.1:n.*567A>G
XM_017019219.2:c.*567A>G	XP_016874708.1:n.*567A>G
NM_000834.5:c.*567A>G MANE Select	NP_000825.2:n.*567A>G