Canonical Allele Identifier: CA603467509
Gene: GRIN2B HGNC NCBI

Linked Data

dbSNP Id: rs1158829859

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981828G>T , CM000674.2:g.13981828G>T GRCh38
NC_000012.11:g.14134762G>T , CM000674.1:g.14134762G>T GRCh37
NC_000012.10:g.14026029G>T NCBI36
NG_031854.1:g.3261C>A
NG_031854.2:g.5185C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000630791.2:c.-683+88C>A ENSP00000486677.2:n.-683+88C>A
ENST00000627535.2:c.-448+88C>A ENSP00000486411.1:n.-448+88C>A
ENST00000630791.1:c.-683+88C>A ENSP00000486677.1:n.-683+88C>A
XM_011520629.1:c.-683+88C>A XP_011518931.1:n.-683+88C>A
XM_011520628.2:c.-934C>A XP_011518930.1:n.-934C>A
XM_011520629.2:c.-683+88C>A XP_011518931.1:n.-683+88C>A