Canonical Allele Identifier: CA10636863

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 307729
• ClinVar RCV Id: RCV000356347
• dbSNP Id: rs886049096
• gnomAD v4: 12-13562551-A-G
• MyVariant Identifiers: chr12:g.13715485A>G (hg19) ; chr12:g.13562551A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562551A>G , CM000674.2:g.13562551A>G	GRCh38
NC_000012.11:g.13715485A>G , CM000674.1:g.13715485A>G	GRCh37
NC_000012.10:g.13606752A>G	NCBI36
NG_031854.1:g.422538T>C
NG_031854.2:g.424462T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.*232T>C MANE Select	ENSP00000477455.1:n.*232T>C
ENST00000637214.1:c.69+46052T>C	ENSP00000489997.1:n.69+46052T>C
ENST00000609686.3:c.*232T>C	ENSP00000477455.1:n.*232T>C
NM_000834.3:c.*232T>C	NP_000825.2:n.*232T>C
XM_005253351.2:c.*232T>C	XP_005253408.1:n.*232T>C
XM_011520628.1:c.*232T>C	XP_011518930.1:n.*232T>C
XM_011520629.1:c.*232T>C	XP_011518931.1:n.*232T>C
XM_011520630.1:c.*232T>C	XP_011518932.1:n.*232T>C
NM_000834.4:c.*232T>C	NP_000825.2:n.*232T>C
XM_005253351.3:c.*232T>C	XP_005253408.1:n.*232T>C
XM_011520628.2:c.*232T>C	XP_011518930.1:n.*232T>C
XM_011520629.2:c.*232T>C	XP_011518931.1:n.*232T>C
XM_017019219.2:c.*232T>C	XP_016874708.1:n.*232T>C
NM_000834.5:c.*232T>C MANE Select	NP_000825.2:n.*232T>C