Canonical Allele Identifier: CA406698241
Gene: GRIN2D HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419719G>C , CM000681.2:g.48419719G>C GRCh38
NC_000019.9:g.48922976G>C , CM000681.1:g.48922976G>C GRCh37
NC_000019.8:g.53614788G>C NCBI36
NG_052829.1:g.29845G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1996G>C MANE Select ENSP00000263269.2:p.Ala666Pro
ENST00000263269.3:c.1996G>C ENSP00000263269.2:p.Ala666Pro
NM_000836.2:c.1996G>C NP_000827.2:p.Ala666Pro
XM_011526872.1:c.1996G>C XP_011525174.1:p.Ala666Pro
NM_000836.4:c.1996G>C MANE Select NP_000827.2:p.Ala666Pro