Canonical Allele Identifier: CA603467508
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs557661981
gnomAD v2: 12-14134751-G-T
gnomAD v3: 12-13981817-G-T
gnomAD v4: 12-13981817-G-T
MyVariant Identifiers: chr12:g.14134751G>T (hg19) chr12:g.13981817G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981817G>T , CM000674.2:g.13981817G>T GRCh38
NC_000012.11:g.14134751G>T , CM000674.1:g.14134751G>T GRCh37
NC_000012.10:g.14026018G>T NCBI36
NG_031854.1:g.3272C>A
NG_031854.2:g.5196C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000630791.2:c.-683+99C>A ENSP00000486677.2:n.-683+99C>A
ENST00000627535.2:c.-448+99C>A ENSP00000486411.1:n.-448+99C>A
ENST00000630791.1:c.-683+99C>A ENSP00000486677.1:n.-683+99C>A
XM_011520629.1:c.-683+99C>A XP_011518931.1:n.-683+99C>A
XM_011520628.2:c.-923C>A XP_011518930.1:n.-923C>A
XM_011520629.2:c.-683+99C>A XP_011518931.1:n.-683+99C>A
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