Canonical Allele Identifier: CA2617758350
Gene: GRIN2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13981678C>A , CM000674.2:g.13981678C>A GRCh38
NC_000012.11:g.14134612C>A , CM000674.1:g.14134612C>A GRCh37
NC_000012.10:g.14025879C>A NCBI36
NG_031854.1:g.3411G>T
NG_031854.2:g.5335G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000630791.2:c.-682-102G>T ENSP00000486677.2:n.-682-102G>T
ENST00000627535.2:c.-448+238G>T ENSP00000486411.1:n.-448+238G>T
ENST00000630791.1:c.-682-102G>T ENSP00000486677.1:n.-682-102G>T
XM_011520629.1:c.-682-102G>T XP_011518931.1:n.-682-102G>T
XM_011520628.2:c.-784G>T XP_011518930.1:n.-784G>T
XM_011520629.2:c.-682-102G>T XP_011518931.1:n.-682-102G>T