Canonical Allele Identifier: CA406698417
Gene: GRIN2D HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.48923051T>A (hg19) chr19:g.48419794T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419794T>A , CM000681.2:g.48419794T>A GRCh38
NC_000019.9:g.48923051T>A , CM000681.1:g.48923051T>A GRCh37
NC_000019.8:g.53614863T>A NCBI36
NG_052829.1:g.29920T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.2071T>A MANE Select ENSP00000263269.2:p.Ser691Thr
ENST00000263269.3:c.2071T>A ENSP00000263269.2:p.Ser691Thr
NM_000836.2:c.2071T>A NP_000827.2:p.Ser691Thr
XM_011526872.1:c.2071T>A XP_011525174.1:p.Ser691Thr
NM_000836.4:c.2071T>A MANE Select NP_000827.2:p.Ser691Thr
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