Canonical Allele Identifier: CA685703368

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1193003716
• gnomAD v3: 12-13981734-A-C
• gnomAD v4: 12-13981734-A-C
• MyVariant Identifiers: chr12:g.14134668A>C (hg19) ; chr12:g.13981734A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13981734A>C , CM000674.2:g.13981734A>C	GRCh38
NC_000012.11:g.14134668A>C , CM000674.1:g.14134668A>C	GRCh37
NC_000012.10:g.14025935A>C	NCBI36
NG_031854.1:g.3355T>G
NG_031854.2:g.5279T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000630791.2:c.-682-158T>G	ENSP00000486677.2:n.-682-158T>G
ENST00000627535.2:c.-448+182T>G	ENSP00000486411.1:n.-448+182T>G
ENST00000630791.1:c.-682-158T>G	ENSP00000486677.1:n.-682-158T>G
XM_011520629.1:c.-682-158T>G	XP_011518931.1:n.-682-158T>G
XM_011520628.2:c.-840T>G	XP_011518930.1:n.-840T>G
XM_011520629.2:c.-682-158T>G	XP_011518931.1:n.-682-158T>G