Canonical Allele Identifier: CA406698302
Gene: GRIN2D HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.2021C>G MANE Select ENSP00000263269.2:p.Thr674Arg
ENST00000263269.3:c.2021C>G ENSP00000263269.2:p.Thr674Arg
NM_000836.2:c.2021C>G NP_000827.2:p.Thr674Arg
XM_011526872.1:c.2021C>G XP_011525174.1:p.Thr674Arg
NM_000836.4:c.2021C>G MANE Select NP_000827.2:p.Thr674Arg