Canonical Allele Identifier: CA2794601235

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562215A>T , CM000674.2:g.13562215A>T	GRCh38
NC_000012.11:g.13715149A>T , CM000674.1:g.13715149A>T	GRCh37
NC_000012.10:g.13606416A>T	NCBI36
NG_031854.1:g.422874T>A
NG_031854.2:g.424798T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*568T>A MANE Select	ENSP00000477455.1:n.*568T>A
ENST00000636207.1:n.54+23T>A
ENST00000637214.1:c.69+46388T>A	ENSP00000489997.1:n.69+46388T>A
ENST00000609686.3:c.*568T>A	ENSP00000477455.1:n.*568T>A
NM_000834.3:c.*568T>A	NP_000825.2:n.*568T>A
XM_005253351.2:c.*568T>A	XP_005253408.1:n.*568T>A
XM_011520628.1:c.*568T>A	XP_011518930.1:n.*568T>A
XM_011520629.1:c.*568T>A	XP_011518931.1:n.*568T>A
XM_011520630.1:c.*568T>A	XP_011518932.1:n.*568T>A
NM_000834.4:c.*568T>A	NP_000825.2:n.*568T>A
XM_005253351.3:c.*568T>A	XP_005253408.1:n.*568T>A
XM_011520628.2:c.*568T>A	XP_011518930.1:n.*568T>A
XM_011520629.2:c.*568T>A	XP_011518931.1:n.*568T>A
XM_017019219.2:c.*568T>A	XP_016874708.1:n.*568T>A
NM_000834.5:c.*568T>A MANE Select	NP_000825.2:n.*568T>A