Canonical Allele Identifier: CA685728226

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1300217443
• gnomAD v3: 12-13944734-G-C
• gnomAD v4: 12-13944734-G-C
• MyVariant Identifiers: chr12:g.14097668G>C (hg19) ; chr12:g.13944734G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13944734G>C , CM000674.2:g.13944734G>C	GRCh38
NC_000012.11:g.14097668G>C , CM000674.1:g.14097668G>C	GRCh37
NC_000012.10:g.13988935G>C	NCBI36
NG_031854.1:g.40355C>G
NG_031854.2:g.42279C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000609686.4:c.-19+35194C>G MANE Select	ENSP00000477455.1:n.-19+35194C>G
ENST00000630791.2:c.-19+35194C>G	ENSP00000486677.2:n.-19+35194C>G
ENST00000609686.3:c.-19+35194C>G	ENSP00000477455.1:n.-19+35194C>G
ENST00000627535.2:c.-19+35194C>G	ENSP00000486411.1:n.-19+35194C>G
ENST00000630791.1:c.-19+35194C>G	ENSP00000486677.1:n.-19+35194C>G
NM_000834.3:c.-19+35194C>G	NP_000825.2:n.-19+35194C>G
XM_011520628.1:c.-19+35194C>G	XP_011518930.1:n.-19+35194C>G
XM_011520629.1:c.-19+35194C>G	XP_011518931.1:n.-19+35194C>G
XM_011520630.1:c.-19+35194C>G	XP_011518932.1:n.-19+35194C>G
NM_000834.4:c.-19+35194C>G	NP_000825.2:n.-19+35194C>G
XM_011520628.2:c.-19+35194C>G	XP_011518930.1:n.-19+35194C>G
XM_011520629.2:c.-19+35194C>G	XP_011518931.1:n.-19+35194C>G
XM_017019219.2:c.-19+35194C>G	XP_016874708.1:n.-19+35194C>G
NM_000834.5:c.-19+35194C>G MANE Select	NP_000825.2:n.-19+35194C>G