Canonical Allele Identifier: CA406698301
Gene: GRIN2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419744C>A , CM000681.2:g.48419744C>A GRCh38
NC_000019.9:g.48923001C>A , CM000681.1:g.48923001C>A GRCh37
NC_000019.8:g.53614813C>A NCBI36
NG_052829.1:g.29870C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.2021C>A MANE Select ENSP00000263269.2:p.Thr674Lys
ENST00000263269.3:c.2021C>A ENSP00000263269.2:p.Thr674Lys
NM_000836.2:c.2021C>A NP_000827.2:p.Thr674Lys
XM_011526872.1:c.2021C>A XP_011525174.1:p.Thr674Lys
NM_000836.4:c.2021C>A MANE Select NP_000827.2:p.Thr674Lys