Canonical Allele Identifier: CA2617751794

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13615705-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13615708del , CM000674.2:g.13615708del	GRCh38
NC_000012.11:g.13768642del , CM000674.1:g.13768642del	GRCh37
NC_000012.10:g.13659909del	NCBI36
NG_031854.1:g.369383del
NG_031854.2:g.371307del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.1329-42del MANE Select	ENSP00000477455.1:n.1329-42del
ENST00000630791.2:c.1329-42del	ENSP00000486677.2:n.1329-42del
ENST00000609686.3:c.1329-42del	ENSP00000477455.1:n.1329-42del
NM_000834.3:c.1329-42del	NP_000825.2:n.1329-42del
XM_011520628.1:c.1329-42del	XP_011518930.1:n.1329-42del
XM_011520629.1:c.1329-42del	XP_011518931.1:n.1329-42del
XM_011520630.1:c.1329-42del	XP_011518932.1:n.1329-42del
XR_931372.1:n.307+482del
XR_931373.1:n.447+482del
XR_931374.1:n.246+482del
NM_000834.4:c.1329-42del	NP_000825.2:n.1329-42del
XM_011520628.2:c.1329-42del	XP_011518930.1:n.1329-42del
XM_011520629.2:c.1329-42del	XP_011518931.1:n.1329-42del
XM_017019219.2:c.1329-42del	XP_016874708.1:n.1329-42del
XR_001749013.1:n.728+482del
XR_931372.2:n.444+482del
XR_931373.2:n.586+482del
NM_000834.5:c.1329-42del MANE Select	NP_000825.2:n.1329-42del