Canonical Allele Identifier: CA406697620
Gene: GRIN2D HGNC NCBI

Linked Data

gnomAD v4: 19-48419590-G-A
MyVariant Identifiers: chr19:g.48922847G>A (hg19) chr19:g.48419590G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419590G>A , CM000681.2:g.48419590G>A GRCh38
NC_000019.9:g.48922847G>A , CM000681.1:g.48922847G>A GRCh37
NC_000019.8:g.53614659G>A NCBI36
NG_052829.1:g.29716G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1867G>A MANE Select ENSP00000263269.2:p.Gly623Ser
ENST00000263269.3:c.1867G>A ENSP00000263269.2:p.Gly623Ser
NM_000836.2:c.1867G>A NP_000827.2:p.Gly623Ser
XM_011526872.1:c.1867G>A XP_011525174.1:p.Gly623Ser
NM_000836.4:c.1867G>A MANE Select NP_000827.2:p.Gly623Ser
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Search 100 bp 3'