Canonical Allele Identifier: CA685661424

Gene: GRIN2B

Linked Data

• dbSNP Id: rs201764269
• gnomAD v3: 12-13562342-T-A
• gnomAD v4: 12-13562342-T-A
• MyVariant Identifiers: chr12:g.13715276T>A (hg19) ; chr12:g.13562342T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562342T>A , CM000674.2:g.13562342T>A	GRCh38
NC_000012.11:g.13715276T>A , CM000674.1:g.13715276T>A	GRCh37
NC_000012.10:g.13606543T>A	NCBI36
NG_031854.1:g.422747A>T
NG_031854.2:g.424671A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*441A>T MANE Select	ENSP00000477455.1:n.*441A>T
ENST00000637214.1:c.69+46261A>T	ENSP00000489997.1:n.69+46261A>T
ENST00000609686.3:c.*441A>T	ENSP00000477455.1:n.*441A>T
NM_000834.3:c.*441A>T	NP_000825.2:n.*441A>T
XM_005253351.2:c.*441A>T	XP_005253408.1:n.*441A>T
XM_011520628.1:c.*441A>T	XP_011518930.1:n.*441A>T
XM_011520629.1:c.*441A>T	XP_011518931.1:n.*441A>T
XM_011520630.1:c.*441A>T	XP_011518932.1:n.*441A>T
NM_000834.4:c.*441A>T	NP_000825.2:n.*441A>T
XM_005253351.3:c.*441A>T	XP_005253408.1:n.*441A>T
XM_011520628.2:c.*441A>T	XP_011518930.1:n.*441A>T
XM_011520629.2:c.*441A>T	XP_011518931.1:n.*441A>T
XM_017019219.2:c.*441A>T	XP_016874708.1:n.*441A>T
NM_000834.5:c.*441A>T MANE Select	NP_000825.2:n.*441A>T