Canonical Allele Identifier: CA2339887559
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs1970991997
gnomAD v4: 19-48419565-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419565C>A , CM000681.2:g.48419565C>A GRCh38
NC_000019.9:g.48922822C>A , CM000681.1:g.48922822C>A GRCh37
NC_000019.8:g.53614634C>A NCBI36
NG_052829.1:g.29691C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-20C>A MANE Select ENSP00000263269.2:n.1862-20C>A
ENST00000263269.3:c.1862-20C>A ENSP00000263269.2:n.1862-20C>A
NM_000836.2:c.1862-20C>A NP_000827.2:n.1862-20C>A
XM_011526872.1:c.1862-20C>A XP_011525174.1:n.1862-20C>A
NM_000836.4:c.1862-20C>A MANE Select NP_000827.2:n.1862-20C>A
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