Canonical Allele Identifier: CA406698156
Gene: GRIN2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.48922956T>C (hg19) chr19:g.48419699T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419699T>C , CM000681.2:g.48419699T>C GRCh38
NC_000019.9:g.48922956T>C , CM000681.1:g.48922956T>C GRCh37
NC_000019.8:g.53614768T>C NCBI36
NG_052829.1:g.29825T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1976T>C MANE Select ENSP00000263269.2:p.Val659Ala
ENST00000263269.3:c.1976T>C ENSP00000263269.2:p.Val659Ala
NM_000836.2:c.1976T>C NP_000827.2:p.Val659Ala
XM_011526872.1:c.1976T>C XP_011525174.1:p.Val659Ala
NM_000836.4:c.1976T>C MANE Select NP_000827.2:p.Val659Ala
Search 100 bp 5'
Search 100 bp 3'