Canonical Allele Identifier: CA384053375

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 1762316
• ClinVar RCV Id: RCV002427812
• MyVariant Identifiers: chr12:g.13906444A>C (hg19) ; chr12:g.13753510A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13753510A>C , CM000674.2:g.13753510A>C	GRCh38
NC_000012.11:g.13906444A>C , CM000674.1:g.13906444A>C	GRCh37
NC_000012.10:g.13797711A>C	NCBI36
NG_031854.1:g.231579T>G
NG_031854.2:g.233503T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.817T>G MANE Select	ENSP00000477455.1:p.Phe273Val
ENST00000630791.2:c.817T>G	ENSP00000486677.2:p.Phe273Val
ENST00000609686.3:c.817T>G	ENSP00000477455.1:p.Phe273Val
NM_000834.3:c.817T>G	NP_000825.2:p.Phe273Val
XM_011520628.1:c.817T>G	XP_011518930.1:p.Phe273Val
XM_011520629.1:c.817T>G	XP_011518931.1:p.Phe273Val
XM_011520630.1:c.817T>G	XP_011518932.1:p.Phe273Val
NM_000834.4:c.817T>G	NP_000825.2:p.Phe273Val
XM_011520628.2:c.817T>G	XP_011518930.1:p.Phe273Val
XM_011520629.2:c.817T>G	XP_011518931.1:p.Phe273Val
XM_017019219.2:c.817T>G	XP_016874708.1:p.Phe273Val
NM_000834.5:c.817T>G MANE Select	NP_000825.2:p.Phe273Val