Canonical Allele Identifier: CA406698355
Gene: GRIN2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419768T>A , CM000681.2:g.48419768T>A GRCh38
NC_000019.9:g.48923025T>A , CM000681.1:g.48923025T>A GRCh37
NC_000019.8:g.53614837T>A NCBI36
NG_052829.1:g.29894T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.2045T>A MANE Select ENSP00000263269.2:p.Ile682Asn
ENST00000263269.3:c.2045T>A ENSP00000263269.2:p.Ile682Asn
NM_000836.2:c.2045T>A NP_000827.2:p.Ile682Asn
XM_011526872.1:c.2045T>A XP_011525174.1:p.Ile682Asn
NM_000836.4:c.2045T>A MANE Select NP_000827.2:p.Ile682Asn