Canonical Allele Identifier: CA2617717659

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13561169-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561169C>A , CM000674.2:g.13561169C>A	GRCh38
NC_000012.11:g.13714103C>A , CM000674.1:g.13714103C>A	GRCh37
NC_000012.10:g.13605370C>A	NCBI36
NG_031854.1:g.423920G>T
NG_031854.2:g.425844G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000609686.4:c.*1614G>T MANE Select	ENSP00000477455.1:n.*1614G>T
ENST00000637214.1:c.69+47434G>T	ENSP00000489997.1:n.69+47434G>T
ENST00000609686.3:c.*1614G>T	ENSP00000477455.1:n.*1614G>T
XM_005253351.2:c.*1614G>T	XP_005253408.1:n.*1614G>T
XM_011520628.1:c.*1614G>T	XP_011518930.1:n.*1614G>T
XM_011520629.1:c.*1614G>T	XP_011518931.1:n.*1614G>T
XM_011520630.1:c.*1614G>T	XP_011518932.1:n.*1614G>T
NM_000834.4:c.*1614G>T	NP_000825.2:n.*1614G>T
XM_005253351.3:c.*1614G>T	XP_005253408.1:n.*1614G>T
XM_011520628.2:c.*1614G>T	XP_011518930.1:n.*1614G>T
XM_011520629.2:c.*1614G>T	XP_011518931.1:n.*1614G>T
XM_017019219.2:c.*1614G>T	XP_016874708.1:n.*1614G>T
NM_000834.5:c.*1614G>T MANE Select	NP_000825.2:n.*1614G>T