Canonical Allele Identifier: CA685661589

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1174785437
• gnomAD v3: 12-13562535-A-T
• gnomAD v4: 12-13562535-A-T
• MyVariant Identifiers: chr12:g.13715469A>T (hg19) ; chr12:g.13562535A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562535A>T , CM000674.2:g.13562535A>T	GRCh38
NC_000012.11:g.13715469A>T , CM000674.1:g.13715469A>T	GRCh37
NC_000012.10:g.13606736A>T	NCBI36
NG_031854.1:g.422554T>A
NG_031854.2:g.424478T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*248T>A MANE Select	ENSP00000477455.1:n.*248T>A
ENST00000637214.1:c.69+46068T>A	ENSP00000489997.1:n.69+46068T>A
ENST00000609686.3:c.*248T>A	ENSP00000477455.1:n.*248T>A
NM_000834.3:c.*248T>A	NP_000825.2:n.*248T>A
XM_005253351.2:c.*248T>A	XP_005253408.1:n.*248T>A
XM_011520628.1:c.*248T>A	XP_011518930.1:n.*248T>A
XM_011520629.1:c.*248T>A	XP_011518931.1:n.*248T>A
XM_011520630.1:c.*248T>A	XP_011518932.1:n.*248T>A
NM_000834.4:c.*248T>A	NP_000825.2:n.*248T>A
XM_005253351.3:c.*248T>A	XP_005253408.1:n.*248T>A
XM_011520628.2:c.*248T>A	XP_011518930.1:n.*248T>A
XM_011520629.2:c.*248T>A	XP_011518931.1:n.*248T>A
XM_017019219.2:c.*248T>A	XP_016874708.1:n.*248T>A
NM_000834.5:c.*248T>A MANE Select	NP_000825.2:n.*248T>A