Canonical Allele Identifier: CA2339887607
Gene: GRIN2D HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419721C= , CM000681.2:g.48419721C= GRCh38
NC_000019.9:g.48922978C= , CM000681.1:g.48922978C= GRCh37
NC_000019.8:g.53614790C= NCBI36
NG_052829.1:g.29847C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1998C= MANE Select ENSP00000263269.2:p.Ala666=
ENST00000263269.3:c.1998C= ENSP00000263269.2:p.Ala666=
NM_000836.2:c.1998C= NP_000827.2:p.Ala666=
XM_011526872.1:c.1998C= XP_011525174.1:p.Ala666=
NM_000836.4:c.1998C= MANE Select NP_000827.2:p.Ala666=