Canonical Allele Identifier: CA2017631045
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1863142063
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981733A>T , CM000674.2:g.13981733A>T GRCh38
NC_000012.11:g.14134667A>T , CM000674.1:g.14134667A>T GRCh37
NC_000012.10:g.14025934A>T NCBI36
NG_031854.1:g.3356T>A
NG_031854.2:g.5280T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000630791.2:c.-682-157T>A ENSP00000486677.2:n.-682-157T>A
ENST00000627535.2:c.-448+183T>A ENSP00000486411.1:n.-448+183T>A
ENST00000630791.1:c.-682-157T>A ENSP00000486677.1:n.-682-157T>A
XM_011520629.1:c.-682-157T>A XP_011518931.1:n.-682-157T>A
XM_011520628.2:c.-839T>A XP_011518930.1:n.-839T>A
XM_011520629.2:c.-682-157T>A XP_011518931.1:n.-682-157T>A
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