Canonical Allele Identifier: CA2530602431

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611439C>T , CM000674.2:g.13611439C>T	GRCh38
NC_000012.11:g.13764373C>T , CM000674.1:g.13764373C>T	GRCh37
NC_000012.10:g.13655640C>T	NCBI36
NG_031854.1:g.373650G>A
NG_031854.2:g.375574G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1780+286G>A MANE Select	ENSP00000477455.1:n.1780+286G>A
ENST00000609686.3:c.1780+286G>A	ENSP00000477455.1:n.1780+286G>A
NM_000834.3:c.1780+286G>A	NP_000825.2:n.1780+286G>A
XM_011520628.1:c.1780+286G>A	XP_011518930.1:n.1780+286G>A
XM_011520629.1:c.1780+286G>A	XP_011518931.1:n.1780+286G>A
XM_011520630.1:c.1780+286G>A	XP_011518932.1:n.1780+286G>A
XR_931372.1:n.179-3659C>T
XR_931373.1:n.318+2682C>T
XR_931374.1:n.117+839C>T
NM_000834.4:c.1780+286G>A	NP_000825.2:n.1780+286G>A
XM_011520628.2:c.1780+286G>A	XP_011518930.1:n.1780+286G>A
XM_011520629.2:c.1780+286G>A	XP_011518931.1:n.1780+286G>A
XM_017019219.2:c.1780+286G>A	XP_016874708.1:n.1780+286G>A
XR_001749013.1:n.599+839C>T
XR_931372.2:n.316-3659C>T
XR_931373.2:n.457+2682C>T
NM_000834.5:c.1780+286G>A MANE Select	NP_000825.2:n.1780+286G>A