Canonical Allele Identifier: CA406698307
Gene: GRIN2D HGNC NCBI

Linked Data

ClinVar Variation Id: 1499341
ClinVar RCV Id: RCV002010598
dbSNP Id: rs1600982197
MyVariant Identifiers: chr19:g.48923004C>A (hg19) chr19:g.48419747C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419747C>A , CM000681.2:g.48419747C>A GRCh38
NC_000019.9:g.48923004C>A , CM000681.1:g.48923004C>A GRCh37
NC_000019.8:g.53614816C>A NCBI36
NG_052829.1:g.29873C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.2024C>A MANE Select ENSP00000263269.2:p.Ala675Asp
ENST00000263269.3:c.2024C>A ENSP00000263269.2:p.Ala675Asp
NM_000836.2:c.2024C>A NP_000827.2:p.Ala675Asp
XM_011526872.1:c.2024C>A XP_011525174.1:p.Ala675Asp
NM_000836.4:c.2024C>A MANE Select NP_000827.2:p.Ala675Asp
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Search 100 bp 3'