Canonical Allele Identifier: CA406698187
Gene: GRIN2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419708G>T , CM000681.2:g.48419708G>T GRCh38
NC_000019.9:g.48922965G>T , CM000681.1:g.48922965G>T GRCh37
NC_000019.8:g.53614777G>T NCBI36
NG_052829.1:g.29834G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1985G>T MANE Select ENSP00000263269.2:p.Trp662Leu
ENST00000263269.3:c.1985G>T ENSP00000263269.2:p.Trp662Leu
NM_000836.2:c.1985G>T NP_000827.2:p.Trp662Leu
XM_011526872.1:c.1985G>T XP_011525174.1:p.Trp662Leu
NM_000836.4:c.1985G>T MANE Select NP_000827.2:p.Trp662Leu