Canonical Allele Identifier: CA996593783
Gene: GRIN2D HGNC NCBI

Linked Data

dbSNP Id: rs950043936
gnomAD v3: 19-48419511-C-G
gnomAD v4: 19-48419511-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48419511C>G , CM000681.2:g.48419511C>G GRCh38
NC_000019.9:g.48922768C>G , CM000681.1:g.48922768C>G GRCh37
NC_000019.8:g.53614580C>G NCBI36
NG_052829.1:g.29637C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263269.4:c.1862-74C>G MANE Select ENSP00000263269.2:n.1862-74C>G
ENST00000263269.3:c.1862-74C>G ENSP00000263269.2:n.1862-74C>G
NM_000836.2:c.1862-74C>G NP_000827.2:n.1862-74C>G
XM_011526872.1:c.1862-74C>G XP_011525174.1:n.1862-74C>G
NM_000836.4:c.1862-74C>G MANE Select NP_000827.2:n.1862-74C>G
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