Canonical Allele Identifier: CA685703374

Gene: GRIN2B

Linked Data

• dbSNP Id: rs1251763214
• gnomAD v3: 12-13981744-G-C
• gnomAD v4: 12-13981744-G-C
• MyVariant Identifiers: chr12:g.14134678G>C (hg19) ; chr12:g.13981744G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.13981744G>C , CM000674.2:g.13981744G>C	GRCh38
NC_000012.11:g.14134678G>C , CM000674.1:g.14134678G>C	GRCh37
NC_000012.10:g.14025945G>C	NCBI36
NG_031854.1:g.3345C>G
NG_031854.2:g.5269C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000630791.2:c.-682-168C>G	ENSP00000486677.2:n.-682-168C>G
ENST00000627535.2:c.-448+172C>G	ENSP00000486411.1:n.-448+172C>G
ENST00000630791.1:c.-682-168C>G	ENSP00000486677.1:n.-682-168C>G
XM_011520629.1:c.-682-168C>G	XP_011518931.1:n.-682-168C>G
XM_011520628.2:c.-850C>G	XP_011518930.1:n.-850C>G
XM_011520629.2:c.-682-168C>G	XP_011518931.1:n.-682-168C>G