Canonical Allele Identifier: CA233161336
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1024322473
gnomAD v3: 12-13981752-C-G
gnomAD v4: 12-13981752-C-G
MyVariant Identifiers: chr12:g.14134686C>G (hg19) chr12:g.13981752C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981752C>G , CM000674.2:g.13981752C>G GRCh38
NC_000012.11:g.14134686C>G , CM000674.1:g.14134686C>G GRCh37
NC_000012.10:g.14025953C>G NCBI36
NG_031854.1:g.3337G>C
NG_031854.2:g.5261G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000630791.2:c.-683+164G>C ENSP00000486677.2:n.-683+164G>C
ENST00000627535.2:c.-448+164G>C ENSP00000486411.1:n.-448+164G>C
ENST00000630791.1:c.-683+164G>C ENSP00000486677.1:n.-683+164G>C
XM_011520629.1:c.-683+164G>C XP_011518931.1:n.-683+164G>C
XM_011520628.2:c.-858G>C XP_011518930.1:n.-858G>C
XM_011520629.2:c.-683+164G>C XP_011518931.1:n.-683+164G>C
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