Canonical Allele Identifier: CA2617717582

Gene: GRIN2B

Linked Data

• gnomAD v4: 12-13561042-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13561042G>A , CM000674.2:g.13561042G>A	GRCh38
NC_000012.11:g.13713976G>A , CM000674.1:g.13713976G>A	GRCh37
NC_000012.10:g.13605243G>A	NCBI36
NG_031854.1:g.424047C>T
NG_031854.2:g.425971C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*1741C>T MANE Select	ENSP00000477455.1:n.*1741C>T
ENST00000637214.1:c.69+47561C>T	ENSP00000489997.1:n.69+47561C>T
ENST00000609686.3:c.*1741C>T	ENSP00000477455.1:n.*1741C>T
XM_005253351.2:c.*1741C>T	XP_005253408.1:n.*1741C>T
XM_011520628.1:c.*1741C>T	XP_011518930.1:n.*1741C>T
XM_011520629.1:c.*1741C>T	XP_011518931.1:n.*1741C>T
XM_011520630.1:c.*1741C>T	XP_011518932.1:n.*1741C>T
NM_000834.4:c.*1741C>T	NP_000825.2:n.*1741C>T
XM_005253351.3:c.*1741C>T	XP_005253408.1:n.*1741C>T
XM_011520628.2:c.*1741C>T	XP_011518930.1:n.*1741C>T
XM_011520629.2:c.*1741C>T	XP_011518931.1:n.*1741C>T
XM_017019219.2:c.*1741C>T	XP_016874708.1:n.*1741C>T
NM_000834.5:c.*1741C>T MANE Select	NP_000825.2:n.*1741C>T