Canonical Allele Identifier: CA2581062537

Gene: GRIN2B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13611647A>C , CM000674.2:g.13611647A>C	GRCh38
NC_000012.11:g.13764581A>C , CM000674.1:g.13764581A>C	GRCh37
NC_000012.10:g.13655848A>C	NCBI36
NG_031854.1:g.373442T>G
NG_031854.2:g.375366T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.1780+78T>G MANE Select	ENSP00000477455.1:n.1780+78T>G
ENST00000609686.3:c.1780+78T>G	ENSP00000477455.1:n.1780+78T>G
NM_000834.3:c.1780+78T>G	NP_000825.2:n.1780+78T>G
XM_011520628.1:c.1780+78T>G	XP_011518930.1:n.1780+78T>G
XM_011520629.1:c.1780+78T>G	XP_011518931.1:n.1780+78T>G
XM_011520630.1:c.1780+78T>G	XP_011518932.1:n.1780+78T>G
XR_931372.1:n.179-3451A>C
XR_931373.1:n.318+2890A>C
XR_931374.1:n.117+1047A>C
NM_000834.4:c.1780+78T>G	NP_000825.2:n.1780+78T>G
XM_011520628.2:c.1780+78T>G	XP_011518930.1:n.1780+78T>G
XM_011520629.2:c.1780+78T>G	XP_011518931.1:n.1780+78T>G
XM_017019219.2:c.1780+78T>G	XP_016874708.1:n.1780+78T>G
XR_001749013.1:n.599+1047A>C
XR_931372.2:n.316-3451A>C
XR_931373.2:n.457+2890A>C
NM_000834.5:c.1780+78T>G MANE Select	NP_000825.2:n.1780+78T>G