Canonical Allele Identifier: CA6461471
Gene: GRIN2B HGNC NCBI

Linked Data

ClinVar Variation Id: 833797
dbSNP Id: rs765133670

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.13866171C>A , CM000674.2:g.13866171C>A GRCh38
NC_000012.11:g.14019105C>A , CM000674.1:g.14019105C>A GRCh37
NC_000012.10:g.13910372C>A NCBI36
NG_031854.1:g.118918G>T
NG_031854.2:g.120842G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000609686.4:c.38G>T MANE Select ENSP00000477455.1:p.Trp13Leu
ENST00000630791.2:c.38G>T ENSP00000486677.2:p.Trp13Leu
ENST00000609686.3:c.38G>T ENSP00000477455.1:p.Trp13Leu
ENST00000627535.2:c.38G>T ENSP00000486411.1:p.Trp13Leu
ENST00000630791.1:c.38G>T ENSP00000486677.1:p.Trp13Leu
NM_000834.3:c.38G>T NP_000825.2:p.Trp13Leu
XM_011520628.1:c.38G>T XP_011518930.1:p.Trp13Leu
XM_011520629.1:c.38G>T XP_011518931.1:p.Trp13Leu
XM_011520630.1:c.38G>T XP_011518932.1:p.Trp13Leu
NM_000834.4:c.38G>T NP_000825.2:p.Trp13Leu
XM_011520628.2:c.38G>T XP_011518930.1:p.Trp13Leu
XM_011520629.2:c.38G>T XP_011518931.1:p.Trp13Leu
XM_017019219.2:c.38G>T XP_016874708.1:p.Trp13Leu
NM_000834.5:c.38G>T MANE Select NP_000825.2:p.Trp13Leu