Canonical Allele Identifier: CA2339887600
Gene: GRIN2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419679A= , CM000681.2:g.48419679A= GRCh38
NC_000019.9:g.48922936A= , CM000681.1:g.48922936A= GRCh37
NC_000019.8:g.53614748A= NCBI36
NG_052829.1:g.29805A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1956A= MANE Select ENSP00000263269.2:p.Gly652=
ENST00000263269.3:c.1956A= ENSP00000263269.2:p.Gly652=
NM_000836.2:c.1956A= NP_000827.2:p.Gly652=
XM_011526872.1:c.1956A= XP_011525174.1:p.Gly652=
NM_000836.4:c.1956A= MANE Select NP_000827.2:p.Gly652=