Canonical Allele Identifier: CA406698291
Gene: GRIN2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419740T>C , CM000681.2:g.48419740T>C GRCh38
NC_000019.9:g.48922997T>C , CM000681.1:g.48922997T>C GRCh37
NC_000019.8:g.53614809T>C NCBI36
NG_052829.1:g.29866T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.2017T>C MANE Select ENSP00000263269.2:p.Tyr673His
ENST00000263269.3:c.2017T>C ENSP00000263269.2:p.Tyr673His
NM_000836.2:c.2017T>C NP_000827.2:p.Tyr673His
XM_011526872.1:c.2017T>C XP_011525174.1:p.Tyr673His
NM_000836.4:c.2017T>C MANE Select NP_000827.2:p.Tyr673His