Canonical Allele Identifier: CA383985493

Gene: GRIN2B

Linked Data

• ClinVar Variation Id: 569867
• ClinVar RCV Id: RCV000690599 ; RCV001330053
• dbSNP Id: rs1565452616
• gnomAD v4: 12-13562931-C-G
• MyVariant Identifiers: chr12:g.13715865C>G (hg19) ; chr12:g.13562931C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13562931C>G , CM000674.2:g.13562931C>G	GRCh38
NC_000012.11:g.13715865C>G , CM000674.1:g.13715865C>G	GRCh37
NC_000012.10:g.13607132C>G	NCBI36
NG_031854.1:g.422158G>C
NG_031854.2:g.424082G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.4307G>C MANE Select	ENSP00000477455.1:p.Gly1436Ala
ENST00000637214.1:c.69+45672G>C	ENSP00000489997.1:n.69+45672G>C
ENST00000609686.3:c.4307G>C	ENSP00000477455.1:p.Gly1436Ala
ENST00000628166.1:n.2567G>C
NM_000834.3:c.4307G>C	NP_000825.2:p.Gly1436Ala
XM_005253351.2:c.2093G>C	XP_005253408.1:p.Gly698Ala
XM_011520628.1:c.4307G>C	XP_011518930.1:p.Gly1436Ala
XM_011520629.1:c.4307G>C	XP_011518931.1:p.Gly1436Ala
XM_011520630.1:c.4307G>C	XP_011518932.1:p.Gly1436Ala
NM_000834.4:c.4307G>C	NP_000825.2:p.Gly1436Ala
XM_005253351.3:c.2093G>C	XP_005253408.1:p.Gly698Ala
XM_011520628.2:c.4307G>C	XP_011518930.1:p.Gly1436Ala
XM_011520629.2:c.4307G>C	XP_011518931.1:p.Gly1436Ala
XM_017019219.2:c.4307G>C	XP_016874708.1:p.Gly1436Ala
NM_000834.5:c.4307G>C MANE Select	NP_000825.2:p.Gly1436Ala